Search by Gene
| Item | Value |
|---|---|
| geneid | 9429 |
| ensemblid | ENSG00000118777.12 |
| hgncid | 74 |
| symbol | ABCG2 |
| name | ATP binding cassette subfamily G member 2 (Junior blood group) |
| refseq_nuc | NM_004827.3 |
| refseq_prot | NP_004818.2 |
| ensembl_nuc | ENST00000237612.8 |
| ensembl_prot | ENSP00000237612.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 88090269 |
| end | 88158639 |
| strand | - |
| ver | v1.2 |
| region | chr4:88090269-88158639 |
| region5000 | chr4:88085269-88163639 |
| regionname0 | ABCG2_chr4_88090269_88158639 |
| regionname5000 | ABCG2_chr4_88085269_88163639 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 655 | 210 | 72 | 44 | 58 | 6 | 28 | ABCG2_chr4_88085269_88163639 | ABCG2 | MSSSN others(650): Show |
chr4 | 88085269 | 88163639 |
| a0002 | 0/0 | 655 | 70 | 6 | 19 | 36 | 3 | 6 | ABCG2_chr4_88085269_88163639 | ABCG2 | MSSSN others(650): Show |
chr4 | 88085269 | 88163639 |
| a0003 | 0/0 | 655 | 60 | 2 | 9 | 42 | 1 | 6 | ABCG2_chr4_88085269_88163639 | ABCG2 | MSSSN others(650): Show |
chr4 | 88085269 | 88163639 |
| a0004 | 0/0 | 125 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | MSSSN others(120): Show |
chr4 | 88085269 | 88163639 |
| a0005 | 0/0 | 655 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | MSSSN others(650): Show |
chr4 | 88085269 | 88163639 |
| a0006 | 0/0 | 655 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | MSSSN others(650): Show |
chr4 | 88085269 | 88163639 |
| a0007 | 0/0 | 655 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | MSSSN others(650): Show |
chr4 | 88085269 | 88163639 |
| a0008 | 0/0 | 655 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | MSSSN others(650): Show |
chr4 | 88085269 | 88163639 |
| a0009 | 0/0 | 655 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | MSSSN others(650): Show |
chr4 | 88085269 | 88163639 |
| a0010 | 0/0 | 655 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | MSSSN others(650): Show |
chr4 | 88085269 | 88163639 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1965 | 206 | 68 | 44 | 58 | 6 | 28 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0001c0005 | 0/0 | 1965 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0002c0002 | 0/0 | 1965 | 61 | 6 | 12 | 34 | 3 | 6 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0002c0004 | 0/0 | 1965 | 9 | 0 | 7 | 2 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0003c0003 | 0/0 | 1965 | 60 | 2 | 9 | 42 | 1 | 6 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0004c0006 | 0/0 | 1965 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0005c0007 | 0/0 | 1965 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0006c0012 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0007c0011 | 0/0 | 1965 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0008c0008 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0009c0009 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 | ||
| a0010c0010 | 0/0 | 1965 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | ATGTC others(1960): Show |
chr4 | 88085269 | 88163639 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4206 | 184 | 61 | 41 | 52 | 6 | 22 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0002 | 0/0 | 4206 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0004 | 0/0 | 4206 | 5 | 1 | 0 | 0 | 0 | 4 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0005 | 0/0 | 4206 | 3 | 1 | 2 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0006 | 0/0 | 4206 | 3 | 3 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0007 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0008 | 0/0 | 4206 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0009 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0010 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0013 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0014 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0001t0016 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0001c0005t0001 | 0/0 | 4206 | 4 | 4 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0002c0002t0001 | 0/0 | 4206 | 25 | 5 | 8 | 8 | 2 | 2 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0002c0002t0002 | 0/0 | 4206 | 33 | 0 | 4 | 26 | 1 | 2 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0002c0002t0004 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0002c0002t0011 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0002c0002t0012 | 0/0 | 4206 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0002c0004t0001 | 0/0 | 4206 | 6 | 0 | 6 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0002c0004t0007 | 0/0 | 4206 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0002c0004t0015 | 0/0 | 4206 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0003c0003t0001 | 0/0 | 4206 | 48 | 1 | 8 | 32 | 1 | 6 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0003c0003t0003 | 0/0 | 4207 | 10 | 0 | 0 | 10 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4202): Show |
chr4 | 88085269 | 88163639 |
| a0003c0003t0004 | 0/0 | 4206 | 2 | 1 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0004c0006t0001 | 0/0 | 4206 | 3 | 0 | 0 | 3 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0005c0007t0001 | 0/0 | 4206 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0006c0012t0001 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0007c0011t0001 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0008c0008t0001 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0009c0009t0001 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| a0010c0010t0001 | 0/0 | 4206 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | AGTGC others(4201): Show |
chr4 | 88085269 | 88163639 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0010 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0007g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0008g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0008g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0009g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0013g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0014g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0001t0016g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0005t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0001c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0011g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0002t0012g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0004t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0004t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0004t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0004t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0004t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0004t0007g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0004t0007g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0002c0004t0015g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0003c0003t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0004c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0004c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0004c0006t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0005c0007t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0006c0012t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0007c0011t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0008c0008t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0009c0009t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| a0010c0010t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | GBR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0247 | EUR | FIN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0292 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0298 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0294 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00609 | hp1 | a0001 | c0001 | t0008 | g0341 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00609 | hp2 | a0003 | c0003 | t0003 | g0252 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00621 | hp2 | a0001 | c0001 | t0008 | g0340 | EAS | CHS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0181 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0216 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0214 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01069 | hp1 | a0005 | c0007 | t0001 | g0005 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01071 | hp1 | a0005 | c0007 | t0001 | g0005 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01071 | hp2 | a0002 | c0004 | t0001 | g0208 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0196 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0212 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0195 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0063 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01169 | hp1 | a0002 | c0004 | t0001 | g0207 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0087 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0220 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0289 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01433 | hp1 | a0002 | c0004 | t0001 | g0248 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0086 | EUR | IBS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0302 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0182 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01943 | hp2 | a0002 | c0004 | t0001 | g0206 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01952 | hp2 | a0002 | c0004 | t0001 | g0323 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01981 | hp1 | a0003 | c0003 | t0004 | g0334 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02027 | hp2 | a0003 | c0003 | t0001 | g0288 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02040 | hp2 | a0003 | c0003 | t0001 | g0290 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02071 | hp1 | a0003 | c0003 | t0003 | g0250 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0297 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0117 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | CDX | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | CDX | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CDX | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02293 | hp1 | a0002 | c0004 | t0001 | g0012 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0054 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02300 | hp2 | a0002 | c0004 | t0015 | g0330 | AMR | PEL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02602 | hp1 | a0002 | c0002 | t0011 | g0045 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0217 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02622 | hp1 | a0001 | c0005 | t0001 | g0079 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02723 | hp1 | a0003 | c0003 | t0004 | g0333 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02735 | hp2 | a0001 | c0001 | t0009 | g0224 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02818 | hp2 | a0006 | c0012 | t0001 | g0030 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0149 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0335 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03041 | hp2 | a0002 | c0002 | t0004 | g0332 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03139 | hp1 | a0001 | c0001 | t0016 | g0331 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03139 | hp2 | a0001 | c0005 | t0001 | g0099 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0078 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0215 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03453 | hp2 | a0001 | c0005 | t0001 | g0100 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0337 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0336 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03704 | hp1 | a0003 | c0003 | t0001 | g0178 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03831 | hp2 | a0002 | c0002 | t0012 | g0273 | SAS | BEB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0069 | SAS | BEB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0338 | SAS | STU | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0218 | SAS | STU | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG04184 | hp1 | a0001 | c0001 | t0014 | g0116 | SAS | BEB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | CHB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0308 | EAS | CHB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | CHB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18747 | hp2 | a0008 | c0008 | t0001 | g0049 | EAS | CHB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | YRI | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18939 | hp2 | a0003 | c0003 | t0003 | g0251 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18942 | hp2 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18945 | hp1 | a0003 | c0003 | t0001 | g0284 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18951 | hp1 | a0003 | c0003 | t0001 | g0301 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0291 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18953 | hp2 | a0003 | c0003 | t0001 | g0312 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18956 | hp1 | a0003 | c0003 | t0001 | g0309 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0305 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18961 | hp2 | a0003 | c0003 | t0003 | g0183 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18962 | hp1 | a0004 | c0006 | t0001 | g0314 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18963 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0296 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0311 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18972 | hp1 | a0003 | c0003 | t0001 | g0327 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18975 | hp1 | a0009 | c0009 | t0001 | g0186 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18979 | hp1 | a0003 | c0003 | t0001 | g0287 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0307 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18981 | hp2 | a0002 | c0004 | t0007 | g0344 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18983 | hp2 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0295 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18995 | hp1 | a0003 | c0003 | t0003 | g0253 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0343 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19003 | hp1 | a0003 | c0003 | t0001 | g0306 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19003 | hp2 | a0004 | c0006 | t0001 | g0239 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19005 | hp1 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0084 | AFR | LWK | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0339 | AFR | LWK | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19056 | hp1 | a0010 | c0010 | t0001 | g0260 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19057 | hp1 | a0003 | c0003 | t0001 | g0293 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0303 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19063 | hp2 | a0003 | c0003 | t0001 | g0285 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0315 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19068 | hp1 | a0003 | c0003 | t0001 | g0300 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19068 | hp2 | a0004 | c0006 | t0001 | g0240 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19070 | hp1 | a0003 | c0003 | t0003 | g0313 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19078 | hp1 | a0003 | c0003 | t0001 | g0299 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19079 | hp1 | a0002 | c0004 | t0007 | g0342 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19079 | hp2 | a0003 | c0003 | t0001 | g0304 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19083 | hp1 | a0003 | c0003 | t0001 | g0328 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0283 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19088 | hp1 | a0003 | c0003 | t0003 | g0310 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0085 | AFR | YRI | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0040 | EUR | TSI | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0034 | EUR | TSI | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | GIH | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0043 | SAS | GIH | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0202 | AFR | MSL | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| HG06807 | hp2 | a0007 | c0011 | t0001 | g0190 | AFR | USA | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18955 | hp1 | a0003 | c0003 | t0003 | g0262 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0213 | AFR | USA | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0050 | REF | REF | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0010 | REF | REF | ABCG2_chr4_88085269_88163639 | ABCG2 | chr4 | 88085269 | 88163639 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88090270 | A | G | 1 | a0001 | 4 | HG02572.hp1 HG03139.hp1 NA19043.hp1 others(1): Show |
splice_region_variant | LOW | c.*1964T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | chr4 | 88090270 | |||||||
| chr4:88092380 | A | G | 1 | a0010 | 1 | NA19056.hp1 | missense_variant&splice_region_variant | MODERATE | c.1822T>C | p.Cys608Arg | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | 2095/4206 | 1822/1968 | 608/655 | chr4 | 88092380 | |||
| chr4:88097518 | C | T | 1 | a0005 | 2 | HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.1582G>A | p.Ala528Thr | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/16 | 1855/4206 | 1582/1968 | 528/655 | chr4 | 88097518 | |||
| chr4:88114978 | T | G | 1 | a0007 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.922A>C | p.Asn308His | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/16 | 1195/4206 | 922/1968 | 308/655 | chr4 | 88114978 | |||
| chr4:88118207 | G | C | 1 | a0006 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.743C>G | p.Ser248Cys | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/16 | 1016/4206 | 743/1968 | 248/655 | chr4 | 88118207 | |||
| chr4:88131137 | A | G | 1 | a0010 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.455T>C | p.Met152Thr | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/16 | 728/4206 | 455/1968 | 152/655 | chr4 | 88131137 | |||
| chr4:88131147 | C | G | 1 | a0009 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.445G>C | p.Ala149Pro | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/16 | 718/4206 | 445/1968 | 149/655 | chr4 | 88131147 | |||
| chr4:88131171 | G | T | 2 | a0003a0008 | 61 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
missense_variant | MODERATE | c.421C>A | p.Gln141Lys | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/16 | 694/4206 | 421/1968 | 141/655 | chr4 | 88131171 | |||
| chr4:88131805 | G | A | 1 | a0004 | 3 | NA18962.hp1 NA19003.hp2 NA19068.hp2 |
stop_gained&splice_region_variant | HIGH | c.376C>T | p.Gln126* | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 4/16 | 649/4206 | 376/1968 | 126/655 | chr4 | 88131805 | |||
| chr4:88139962 | C | T | 2 | a0002a0008 | 71 | HG00423.hp2 HG00597.hp2 HG01071.hp2 others(68): Show |
missense_variant | MODERATE | c.34G>A | p.Val12Met | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/16 | 307/4206 | 34/1968 | 12/655 | chr4 | 88139962 |
| view | chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88113399 | C | T | 1 | a0002c0004 | 9 | HG01071.hp2 HG01169.hp1 HG01433.hp1 others(6): Show |
synonymous_variant | LOW | c.1098G>A | p.Glu366Glu | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/16 | 1371/4206 | 1098/1968 | 366/655 | chr4 | 88113399 | |||
| chr4:88131812 | G | A | 1 | a0001c0005 | 4 | HG02622.hp1 HG02976.hp1 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.369C>T | p.Tyr123Tyr | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 4/16 | 642/4206 | 369/1968 | 123/655 | chr4 | 88131812 |
| view | chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88090393 | T | C | 1 | a0002c0002t0011 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1841A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | 1841 | chr4 | 88090393 | ||||||
| chr4:88090508 | C | T | 1 | a0001c0001t0005 | 3 | HG00639.hp1 HG01243.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1726G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | 1726 | chr4 | 88090508 | ||||||
| chr4:88090974 | G | A | 1 | a0001c0001t0013 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1260C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | 1260 | chr4 | 88090974 | ||||||
| chr4:88090983 | A | G | 1 | a0002c0002t0012 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1251T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | 1251 | chr4 | 88090983 | ||||||
| chr4:88091168 | A | G | 3 | a0001c0001t0002a0002c0002t0002a0002c0002t0011 | 37 | HG00423.hp2 HG00597.hp2 HG01516.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1066T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | 1066 | chr4 | 88091168 | ||||||
| chr4:88091870 | T | TA | 1 | a0003c0003t0003 | 10 | HG00609.hp2 HG02071.hp1 NA18939.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*363_*364insT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | 363 | chr4 | 88091870 | ||||||
| chr4:88091883 | A | T | 1 | a0001c0001t0010 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*351T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | 351 | chr4 | 88091883 | ||||||
| chr4:88092111 | A | G | 1 | a0001c0001t0009 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | 123 | chr4 | 88092111 | ||||||
| chr4:88092168 | T | C | 1 | a0001c0001t0014 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 16/16 | 66 | chr4 | 88092168 | ||||||
| chr4:88158395 | T | C | 1 | a0002c0004t0015 | 1 | HG02300.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/16 | chr4 | 88158395 | |||||||
| chr4:88158480 | G | A | 4 | a0001c0001t0004a0001c0001t0016a0002c0002t0004others(1): Show | 9 | HG01981.hp1 HG02723.hp1 HG03017.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-114C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/16 | 18485 | chr4 | 88158480 | ||||||
| chr4:88158495 | G | A | 1 | a0001c0001t0008 | 2 | HG00609.hp1 HG00621.hp2 |
5_prime_UTR_variant | MODIFIER | c.-129C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/16 | 18500 | chr4 | 88158495 | ||||||
| chr4:88158628 | G | A | 2 | a0001c0001t0007a0002c0004t0007 | 3 | NA18981.hp2 NA19000.hp2 NA19079.hp1 |
5_prime_UTR_variant | MODIFIER | c.-262C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/16 | 18633 | chr4 | 88158628 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:88092704 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1821-323T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88092704 | |||||||
| chr4:88093336 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1821-955G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093336 | |||||||
| chr4:88093377 | A | G | 253 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1821-996T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093377 | |||||||
| chr4:88093459 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1821-1078C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093459 | |||||||
| chr4:88093503 | CA | C | 147 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0021others(144): Show | 148 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.1820+1073delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093503 | |||||||
| chr4:88093503 | CAA | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0019others(167): Show | 175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1820+1072_1820+107 others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093503 | |||||||
| chr4:88093503 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1820+1064_1820+107 others(14): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093503 | |||||||
| chr4:88093604 | C | A | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1820+973G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093604 | |||||||
| chr4:88093609 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1820+968G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093609 | |||||||
| chr4:88093634 | T | C | 7 | a0001c0001t0001g0151a0001c0001t0001g0189a0001c0001t0001g0191others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+943A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093634 | |||||||
| chr4:88093689 | C | T | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1820+888G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093689 | |||||||
| chr4:88093938 | C | T | 58 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(55): Show | 59 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1820+639G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88093938 | |||||||
| chr4:88094011 | A | T | 71 | a0001c0001t0001g0026a0001c0001t0001g0075a0001c0001t0001g0083others(68): Show | 71 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1820+566T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88094011 | |||||||
| chr4:88094029 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1820+548C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88094029 | |||||||
| chr4:88094048 | T | C | 3 | a0001c0001t0006g0084a0001c0001t0006g0085a0001c0001t0016g0331 | 3 | HG03139.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1820+529A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88094048 | |||||||
| chr4:88094371 | A | AGACAATT others(156): Show |
1 | a0001c0001t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1820+205_1820+206i others(165): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88094371 | |||||||
| chr4:88094435 | A | C | 1 | a0001c0001t0001g0104 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1820+142T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88094435 | |||||||
| chr4:88094467 | G | A | 36 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0110others(33): Show | 36 | HG00544.hp1 HG01071.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1820+110C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 15/15 | chr4 | 88094467 | |||||||
| chr4:88094705 | C | T | 169 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(166): Show | 172 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1738-46G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 14/15 | chr4 | 88094705 | |||||||
| chr4:88094735 | T | C | 2 | a0001c0001t0006g0084a0001c0001t0006g0085 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1738-76A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 14/15 | chr4 | 88094735 | |||||||
| chr4:88094828 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1738-169T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 14/15 | chr4 | 88094828 | |||||||
| chr4:88095017 | T | C | 1 | a0001c0001t0001g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1738-358A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 14/15 | chr4 | 88095017 | |||||||
| chr4:88095023 | G | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(223): Show | 232 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1738-364C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 14/15 | chr4 | 88095023 | |||||||
| chr4:88095153 | A | T | 4 | a0001c0001t0001g0103a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG02615.hp2 HG03041.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+367T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 14/15 | chr4 | 88095153 | |||||||
| chr4:88095263 | T | C | 1 | a0002c0004t0001g0323 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1737+257A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 14/15 | chr4 | 88095263 | |||||||
| chr4:88095630 | A | G | 255 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(252): Show | 261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.1648-21T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88095630 | |||||||
| chr4:88095751 | A | T | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1648-142T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88095751 | |||||||
| chr4:88095830 | C | G | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1648-221G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88095830 | |||||||
| chr4:88095918 | A | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0103others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1648-309T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88095918 | |||||||
| chr4:88095920 | T | C | 12 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0103others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1648-311A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88095920 | |||||||
| chr4:88096229 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1648-620C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88096229 | |||||||
| chr4:88096547 | T | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0103others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1647+906A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88096547 | |||||||
| chr4:88096750 | TA | T | 10 | a0001c0001t0001g0151a0001c0001t0001g0189a0001c0001t0001g0191others(7): Show | 10 | HG01884.hp2 HG01978.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1647+702delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88096750 | |||||||
| chr4:88096751 | A | T | 1 | a0001c0001t0001g0092 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1647+702T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88096751 | |||||||
| chr4:88096892 | C | T | 6 | a0001c0001t0001g0151a0001c0001t0001g0189a0001c0001t0001g0191others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647+561G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88096892 | |||||||
| chr4:88097093 | G | A | 1 | a0002c0002t0002g0051 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1647+360C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88097093 | |||||||
| chr4:88097144 | A | G | 12 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0103others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1647+309T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88097144 | |||||||
| chr4:88097159 | A | G | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1647+294T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88097159 | |||||||
| chr4:88097413 | A | G | 93 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0048others(90): Show | 95 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1647+40T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 13/15 | chr4 | 88097413 | |||||||
| chr4:88097766 | G | A | 13 | a0003c0003t0001g0286a0003c0003t0001g0287a0003c0003t0001g0288others(10): Show | 13 | HG02027.hp2 NA18612.hp2 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.1493-159C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88097766 | |||||||
| chr4:88097771 | T | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0103others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1493-164A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88097771 | |||||||
| chr4:88098003 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1493-396C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098003 | |||||||
| chr4:88098344 | G | A | 2 | a0002c0002t0001g0040a0003c0003t0001g0218 | 2 | HG04115.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1493-737C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098344 | |||||||
| chr4:88098463 | C | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(16): Show | 19 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1493-856G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098463 | |||||||
| chr4:88098510 | T | C | 1 | a0002c0004t0001g0012 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1492+814A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098510 | |||||||
| chr4:88098575 | A | G | 227 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(224): Show | 233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1492+749T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098575 | |||||||
| chr4:88098583 | A | G | 56 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0166others(53): Show | 59 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1492+741T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098583 | |||||||
| chr4:88098599 | A | AGT | 11 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0103others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1492+723_1492+724d others(4): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098599 | |||||||
| chr4:88098608 | G | A | 227 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(224): Show | 233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.1492+716C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098608 | |||||||
| chr4:88098610 | G | GTA | 63 | a0001c0001t0001g0026a0001c0001t0001g0075a0001c0001t0001g0083others(60): Show | 63 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.1492+712_1492+713d others(4): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098610 | |||||||
| chr4:88098610 | G | GTATA | 7 | a0002c0002t0001g0054a0002c0002t0001g0065a0002c0002t0001g0067others(4): Show | 7 | HG00544.hp1 HG01928.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1492+710_1492+713d others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098610 | |||||||
| chr4:88098645 | G | GAGAT | 71 | a0001c0001t0001g0015a0001c0001t0001g0022a0001c0001t0001g0025others(68): Show | 72 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.1492+675_1492+678d others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098645 | |||||||
| chr4:88098645 | G | GAGATAGA others(1): Show |
106 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(103): Show | 107 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1492+671_1492+678d others(10): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098645 | |||||||
| chr4:88098645 | G | GAGATAGA others(5): Show |
75 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0062others(72): Show | 79 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.1492+667_1492+678d others(14): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098645 | |||||||
| chr4:88098645 | G | GAGATAGA others(9): Show |
15 | a0001c0001t0001g0019a0001c0001t0001g0071a0001c0001t0001g0097others(12): Show | 15 | HG00438.hp2 HG01074.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1492+663_1492+678d others(18): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098645 | |||||||
| chr4:88098645 | G | GAGATAGA others(13): Show |
2 | a0001c0001t0001g0243a0002c0002t0002g0013 | 2 | HG00423.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.1492+659_1492+678d others(22): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098645 | |||||||
| chr4:88098645 | GAGAT | G | 3 | a0001c0001t0001g0083a0001c0001t0001g0115a0001c0001t0001g0174 | 3 | HG02895.hp1 NA18960.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1492+675_1492+678d others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098645 | |||||||
| chr4:88098669 | T | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0103others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1492+655A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098669 | |||||||
| chr4:88098671 | G | GATAGATA others(13): Show |
1 | a0002c0002t0001g0036 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1492+652_1492+653i others(22): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098671 | |||||||
| chr4:88098685 | T | C | 26 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0115others(23): Show | 26 | HG01071.hp2 HG01169.hp1 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.1492+639A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098685 | |||||||
| chr4:88098685 | T | TAGAC | 7 | a0001c0001t0001g0110a0001c0001t0001g0128a0001c0001t0004g0335others(4): Show | 7 | HG01433.hp1 HG02148.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1492+635_1492+638d others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098685 | |||||||
| chr4:88098685 | T | TAGATAGA others(1): Show |
4 | a0001c0001t0001g0026a0002c0002t0001g0063a0002c0004t0001g0012others(1): Show | 4 | HG00544.hp1 HG01109.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1492+638_1492+639i others(10): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098685 | |||||||
| chr4:88098685 | T | TAGATAGA others(5): Show |
5 | a0001c0001t0001g0148a0001c0001t0004g0336a0001c0001t0004g0337others(2): Show | 5 | HG03490.hp2 HG03492.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1492+638_1492+639i others(14): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098685 | |||||||
| chr4:88098781 | A | G | 1 | a0001c0001t0001g0316 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1492+543T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098781 | |||||||
| chr4:88098973 | G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0006g0084others(2): Show | 5 | HG02486.hp2 HG02886.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1492+351C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88098973 | |||||||
| chr4:88099187 | C | A | 2 | a0001c0001t0013g0220a0002c0002t0012g0273 | 2 | HG01255.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1492+137G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88099187 | |||||||
| chr4:88099275 | C | A | 57 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0166others(54): Show | 60 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1492+49G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88099275 | |||||||
| chr4:88099286 | C | T | 15 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0151others(12): Show | 15 | HG00639.hp1 HG01255.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1492+38G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 12/15 | chr4 | 88099286 | |||||||
| chr4:88099467 | T | C | 1 | a0002c0002t0001g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1368-19A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88099467 | |||||||
| chr4:88099583 | C | T | 1 | a0002c0002t0001g0060 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1368-135G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88099583 | |||||||
| chr4:88099615 | C | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0103others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1368-167G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88099615 | |||||||
| chr4:88099782 | G | A | 57 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0166others(54): Show | 60 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1368-334C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88099782 | |||||||
| chr4:88099937 | C | T | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1368-489G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88099937 | |||||||
| chr4:88100077 | A | G | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1368-629T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100077 | |||||||
| chr4:88100098 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1368-650A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100098 | |||||||
| chr4:88100191 | TA | T | 244 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(241): Show | 247 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.1368-744delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100191 | |||||||
| chr4:88100191 | TAA | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0077a0001c0001t0001g0137others(9): Show | 12 | HG01074.hp1 HG01167.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1368-745_1368-744d others(4): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100191 | |||||||
| chr4:88100261 | C | T | 1 | a0003c0003t0001g0215 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1368-813G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100261 | |||||||
| chr4:88100270 | G | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0103others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1368-822C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100270 | |||||||
| chr4:88100287 | G | A | 2 | a0002c0002t0001g0171a0002c0002t0004g0332 | 2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1368-839C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100287 | |||||||
| chr4:88100302 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1368-854G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100302 | |||||||
| chr4:88100345 | C | T | 1 | a0010c0010t0001g0260 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1367+885G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100345 | |||||||
| chr4:88100398 | G | T | 1 | a0003c0003t0001g0305 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1367+832C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100398 | |||||||
| chr4:88100418 | G | A | 1 | a0001c0005t0001g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1367+812C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100418 | |||||||
| chr4:88100490 | G | A | 19 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(16): Show | 19 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1367+740C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100490 | |||||||
| chr4:88100510 | A | T | 1 | a0010c0010t0001g0260 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1367+720T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100510 | |||||||
| chr4:88100522 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1367+708T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100522 | |||||||
| chr4:88100533 | C | T | 237 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(234): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.1367+697G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100533 | |||||||
| chr4:88100554 | A | G | 254 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(251): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.1367+676T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100554 | |||||||
| chr4:88100567 | G | A | 1 | a0002c0004t0001g0206 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1367+663C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100567 | |||||||
| chr4:88100650 | C | CA | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1367+579dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100650 | |||||||
| chr4:88100752 | C | T | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1367+478G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100752 | |||||||
| chr4:88100753 | G | A | 1 | a0002c0002t0002g0009 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1367+477C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100753 | |||||||
| chr4:88100771 | C | T | 4 | a0001c0001t0005g0140a0001c0001t0005g0181a0001c0001t0013g0220others(1): Show | 4 | HG00639.hp1 HG01255.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+459G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100771 | |||||||
| chr4:88100819 | C | T | 1 | a0002c0002t0001g0266 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1367+411G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100819 | |||||||
| chr4:88100931 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1367+299C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88100931 | |||||||
| chr4:88101036 | C | T | 2 | a0001c0001t0013g0220a0002c0002t0012g0273 | 2 | HG01255.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1367+194G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88101036 | |||||||
| chr4:88101210 | C | T | 225 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(222): Show | 231 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1367+20G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88101210 | |||||||
| chr4:88101215 | C | A | 4 | a0001c0001t0001g0103a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | HG02615.hp2 HG03041.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+15G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 11/15 | chr4 | 88101215 | |||||||
| chr4:88101348 | G | A | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1278-29C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88101348 | |||||||
| chr4:88101491 | C | G | 1 | a0001c0001t0009g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1278-172G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88101491 | |||||||
| chr4:88101494 | T | C | 2 | a0002c0002t0002g0041a0002c0002t0002g0052 | 2 | NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1278-175A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88101494 | |||||||
| chr4:88101605 | G | T | 2 | a0001c0001t0005g0140a0001c0001t0005g0181 | 2 | HG00639.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1278-286C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88101605 | |||||||
| chr4:88102072 | G | A | 57 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0166others(54): Show | 60 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1278-753C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102072 | |||||||
| chr4:88102268 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1278-949A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102268 | |||||||
| chr4:88102363 | C | T | 16 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0094others(13): Show | 16 | HG00609.hp1 HG00621.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1278-1044G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102363 | |||||||
| chr4:88102455 | G | T | 1 | a0002c0002t0002g0039 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1278-1136C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102455 | |||||||
| chr4:88102475 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1278-1156T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102475 | |||||||
| chr4:88102482 | G | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0048a0001c0001t0001g0053others(88): Show | 93 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1278-1163C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102482 | |||||||
| chr4:88102544 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1278-1225A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102544 | |||||||
| chr4:88102545 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1278-1226C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102545 | |||||||
| chr4:88102552 | C | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0090a0001c0001t0001g0097others(4): Show | 7 | HG01109.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1278-1233G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102552 | |||||||
| chr4:88102553 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1278-1234C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102553 | |||||||
| chr4:88102589 | C | T | 1 | a0003c0003t0001g0213 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1278-1270G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102589 | |||||||
| chr4:88102595 | C | CA | 238 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(235): Show | 244 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1278-1277dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102595 | |||||||
| chr4:88102595 | C | CAA | 6 | a0001c0001t0001g0119a0001c0001t0001g0204a0001c0001t0004g0339others(3): Show | 6 | HG01981.hp2 HG02486.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278-1278_1278-127 others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102595 | |||||||
| chr4:88102610 | T | A | 6 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0115others(3): Show | 6 | NA18939.hp1 NA18956.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1278-1291A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102610 | |||||||
| chr4:88102736 | T | C | 2 | a0001c0001t0006g0084a0001c0001t0006g0085 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1278-1417A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102736 | |||||||
| chr4:88102862 | T | C | 2 | a0002c0002t0001g0063a0002c0002t0001g0066 | 2 | HG01109.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1278-1543A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88102862 | |||||||
| chr4:88103068 | G | A | 57 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(54): Show | 58 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.1278-1749C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88103068 | |||||||
| chr4:88103226 | T | C | 15 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0077others(12): Show | 15 | HG01993.hp2 HG02040.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1278-1907A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88103226 | |||||||
| chr4:88103272 | A | G | 1 | a0001c0001t0010g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1278-1953T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88103272 | |||||||
| chr4:88103556 | T | C | 241 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(238): Show | 247 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.1278-2237A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88103556 | |||||||
| chr4:88103661 | G | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0027 | 2 | HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1278-2342C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88103661 | |||||||
| chr4:88103874 | A | C | 252 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(249): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.1278-2555T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88103874 | |||||||
| chr4:88103960 | C | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0162a0001c0001t0001g0193others(1): Show | 4 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278-2641G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88103960 | |||||||
| chr4:88103961 | G | A | 8 | a0001c0001t0001g0082a0001c0001t0001g0134a0001c0001t0001g0135others(5): Show | 8 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1278-2642C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88103961 | |||||||
| chr4:88104089 | C | T | 55 | a0001c0001t0001g0163a0001c0001t0001g0166a0002c0002t0001g0002others(52): Show | 58 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1278-2770G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104089 | |||||||
| chr4:88104403 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1277+2781G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104403 | |||||||
| chr4:88104515 | G | A | 31 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0076others(28): Show | 31 | HG01074.hp1 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1277+2669C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104515 | |||||||
| chr4:88104534 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1277+2650C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104534 | |||||||
| chr4:88104663 | G | GA | 204 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(201): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.1277+2520_1277+252 others(5): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104663 | |||||||
| chr4:88104664 | G | A | 207 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(204): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1277+2520C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104664 | |||||||
| chr4:88104664 | G | GA | 39 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0027others(36): Show | 39 | HG01074.hp1 HG01109.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.1277+2519dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104664 | |||||||
| chr4:88104666 | A | AG | 6 | a0001c0001t0005g0087a0001c0001t0005g0140a0001c0001t0005g0181others(3): Show | 6 | HG00639.hp1 HG01243.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1277+2517_1277+251 others(5): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104666 | |||||||
| chr4:88104730 | G | A | 11 | a0001c0001t0001g0151a0001c0001t0001g0189a0001c0001t0001g0191others(8): Show | 11 | HG00639.hp1 HG01243.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1277+2454C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104730 | |||||||
| chr4:88104793 | C | T | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277+2391G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104793 | |||||||
| chr4:88104855 | A | G | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1277+2329T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104855 | |||||||
| chr4:88104957 | C | T | 207 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(204): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1277+2227G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88104957 | |||||||
| chr4:88105276 | A | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0027others(149): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1277+1908T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88105276 | |||||||
| chr4:88105301 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1277+1883T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88105301 | |||||||
| chr4:88105338 | C | T | 1 | a0008c0008t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1277+1846G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88105338 | |||||||
| chr4:88105352 | C | G | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1277+1832G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88105352 | |||||||
| chr4:88105489 | T | A | 1 | a0002c0002t0002g0013 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1277+1695A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88105489 | |||||||
| chr4:88105490 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1277+1694G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88105490 | |||||||
| chr4:88106005 | A | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG00099.hp1 HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1277+1179T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88106005 | |||||||
| chr4:88106015 | G | A | 1 | a0002c0002t0001g0047 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1277+1169C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88106015 | |||||||
| chr4:88106390 | A | G | 210 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(207): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1277+794T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88106390 | |||||||
| chr4:88106588 | A | T | 1 | a0001c0001t0001g0318 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1277+596T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88106588 | |||||||
| chr4:88106642 | G | A | 1 | a0001c0001t0014g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1277+542C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88106642 | |||||||
| chr4:88106688 | G | C | 59 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(56): Show | 60 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1277+496C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88106688 | |||||||
| chr4:88106988 | G | A | 1 | a0002c0002t0001g0060 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1277+196C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88106988 | |||||||
| chr4:88107072 | A | G | 1 | a0002c0002t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1277+112T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88107072 | |||||||
| chr4:88107089 | A | T | 1 | a0003c0003t0001g0315 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1277+95T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88107089 | |||||||
| chr4:88107092 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1277+92T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88107092 | |||||||
| chr4:88107117 | A | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0016g0331 | 3 | HG02486.hp2 HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1277+67T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88107117 | |||||||
| chr4:88107132 | G | A | 2 | a0002c0002t0001g0242a0003c0003t0001g0290 | 2 | HG02040.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1277+52C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 10/15 | chr4 | 88107132 | |||||||
| chr4:88107326 | T | A | 58 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(55): Show | 59 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.1195-60A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88107326 | |||||||
| chr4:88107392 | A | C | 15 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0161others(12): Show | 15 | HG00609.hp1 HG00621.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1195-126T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88107392 | |||||||
| chr4:88107623 | A | G | 56 | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0166others(53): Show | 59 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1195-357T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88107623 | |||||||
| chr4:88107959 | C | T | 2 | a0002c0002t0002g0041a0002c0002t0002g0052 | 2 | NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1195-693G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88107959 | |||||||
| chr4:88108100 | A | C | 253 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1195-834T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108100 | |||||||
| chr4:88108151 | GTTAAT | G | 340 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(337): Show | 346 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.1195-890_1195-886d others(7): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108151 | |||||||
| chr4:88108183 | A | G | 1 | a0001c0001t0010g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1195-917T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108183 | |||||||
| chr4:88108359 | T | TA | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(195): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1195-1094dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108359 | |||||||
| chr4:88108359 | T | TAA | 9 | a0001c0001t0001g0179a0001c0001t0001g0209a0001c0001t0001g0210others(6): Show | 9 | HG04184.hp1 NA18947.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.1195-1095_1195-109 others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108359 | |||||||
| chr4:88108375 | C | A | 7 | a0002c0004t0001g0012a0002c0004t0001g0206a0002c0004t0001g0207others(4): Show | 7 | HG01071.hp2 HG01169.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1195-1109G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108375 | |||||||
| chr4:88108404 | C | T | 1 | a0001c0001t0013g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1195-1138G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108404 | |||||||
| chr4:88108565 | A | G | 36 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0110others(33): Show | 36 | HG00544.hp1 HG01071.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1195-1299T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108565 | |||||||
| chr4:88108603 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1195-1337G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108603 | |||||||
| chr4:88108688 | A | C | 1 | a0002c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1195-1422T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108688 | |||||||
| chr4:88108714 | G | A | 62 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(59): Show | 63 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1195-1448C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108714 | |||||||
| chr4:88108730 | A | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0256a0001c0001t0001g0324 | 3 | NA18972.hp2 NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1195-1464T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108730 | |||||||
| chr4:88108735 | C | G | 258 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1195-1469G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108735 | |||||||
| chr4:88108857 | A | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG00323.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1195-1591T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88108857 | |||||||
| chr4:88109001 | A | AT | 127 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0025others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1195-1736dupA | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88109001 | |||||||
| chr4:88109112 | C | A | 35 | a0001c0001t0002g0081a0001c0001t0002g0236a0001c0001t0002g0237others(32): Show | 36 | HG00423.hp2 HG00597.hp2 HG01952.hp1 others(33): Show |
intron_variant | MODIFIER | c.1195-1846G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88109112 | |||||||
| chr4:88109207 | C | T | 3 | a0002c0002t0001g0040a0002c0002t0002g0086a0002c0002t0012g0273 | 3 | HG01516.hp1 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1195-1941G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88109207 | |||||||
| chr4:88109267 | G | A | 1 | a0002c0002t0002g0280 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1195-2001C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88109267 | |||||||
| chr4:88109287 | C | G | 1 | a0002c0002t0001g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1195-2021G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88109287 | |||||||
| chr4:88109668 | C | A | 1 | a0002c0002t0001g0036 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1195-2402G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88109668 | |||||||
| chr4:88109689 | T | G | 87 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(84): Show | 89 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.1195-2423A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88109689 | |||||||
| chr4:88109768 | C | G | 126 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0053others(123): Show | 129 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1195-2502G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88109768 | |||||||
| chr4:88109808 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1195-2542A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88109808 | |||||||
| chr4:88110161 | C | T | 24 | a0001c0001t0001g0075a0001c0001t0001g0088a0001c0001t0001g0089others(21): Show | 24 | HG00735.hp2 HG01069.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1195-2895G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88110161 | |||||||
| chr4:88110367 | A | G | 67 | a0001c0001t0001g0161a0001c0005t0001g0099a0002c0002t0001g0002others(64): Show | 69 | HG00423.hp2 HG00597.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.1194+2936T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88110367 | |||||||
| chr4:88110434 | T | G | 66 | a0001c0001t0001g0161a0002c0002t0001g0002a0002c0002t0001g0008others(63): Show | 68 | HG00423.hp2 HG00597.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.1194+2869A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88110434 | |||||||
| chr4:88110563 | G | A | 2 | a0001c0001t0004g0336a0001c0001t0004g0337 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1194+2740C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88110563 | |||||||
| chr4:88110822 | A | T | 34 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(31): Show | 34 | HG00609.hp1 HG00621.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.1194+2481T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88110822 | |||||||
| chr4:88110824 | A | T | 34 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(31): Show | 34 | HG00609.hp1 HG00621.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.1194+2479T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88110824 | |||||||
| chr4:88110825 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1194+2478T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88110825 | |||||||
| chr4:88110825 | AT | A | 83 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(80): Show | 85 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1194+2477delA | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88110825 | |||||||
| chr4:88111135 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1194+2168A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111135 | |||||||
| chr4:88111154 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1194+2149T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111154 | |||||||
| chr4:88111230 | TA | T | 83 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(80): Show | 85 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1194+2072delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111230 | |||||||
| chr4:88111286 | C | T | 1 | a0010c0010t0001g0260 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1194+2017G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111286 | |||||||
| chr4:88111299 | T | C | 1 | a0003c0003t0001g0180 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1194+2004A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111299 | |||||||
| chr4:88111527 | T | A | 1 | a0001c0001t0001g0279 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1194+1776A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111527 | |||||||
| chr4:88111527 | T | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0048others(166): Show | 173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1194+1776A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111527 | |||||||
| chr4:88111645 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1194+1658T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111645 | |||||||
| chr4:88111685 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1194+1618A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111685 | |||||||
| chr4:88111741 | G | C | 1 | a0001c0001t0001g0241 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1194+1562C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111741 | |||||||
| chr4:88111766 | T | C | 2 | a0003c0003t0003g0251a0003c0003t0003g0313 | 2 | NA18939.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1194+1537A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111766 | |||||||
| chr4:88111772 | T | C | 1 | a0002c0004t0001g0206 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1194+1531A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88111772 | |||||||
| chr4:88112086 | T | TA | 122 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(119): Show | 125 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1194+1216dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112086 | |||||||
| chr4:88112128 | C | T | 336 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.1194+1175G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112128 | |||||||
| chr4:88112189 | T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0024 | 2 | HG00741.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1194+1114A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112189 | |||||||
| chr4:88112193 | G | A | 1 | a0007c0011t0001g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1194+1110C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112193 | |||||||
| chr4:88112241 | C | A | 3 | a0002c0002t0001g0054a0002c0002t0001g0065a0002c0002t0001g0067 | 3 | HG01928.hp1 HG01981.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1194+1062G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112241 | |||||||
| chr4:88112257 | A | G | 336 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.1194+1046T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112257 | |||||||
| chr4:88112375 | T | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1194+928A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112375 | |||||||
| chr4:88112446 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1194+857G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112446 | |||||||
| chr4:88112450 | CCT | C | 68 | a0001c0001t0001g0062a0001c0001t0001g0161a0002c0002t0001g0002others(65): Show | 70 | HG00423.hp2 HG00597.hp2 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.1194+851_1194+852d others(4): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112450 | |||||||
| chr4:88112509 | G | C | 35 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(32): Show | 35 | HG00609.hp1 HG00621.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1194+794C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112509 | |||||||
| chr4:88112517 | T | C | 1 | a0001c0001t0001g0318 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1194+786A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112517 | |||||||
| chr4:88112628 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1194+675T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88112628 | |||||||
| chr4:88113012 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1194+291T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88113012 | |||||||
| chr4:88113079 | C | G | 66 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0053others(63): Show | 67 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1194+224G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88113079 | |||||||
| chr4:88113258 | C | A | 1 | a0001c0001t0010g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1194+45G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 9/15 | chr4 | 88113258 | |||||||
| chr4:88113695 | G | C | 47 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0075others(44): Show | 47 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.944-142C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88113695 | |||||||
| chr4:88113733 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.944-180G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88113733 | |||||||
| chr4:88113835 | G | A | 1 | a0002c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.944-282C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88113835 | |||||||
| chr4:88113947 | G | A | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.944-394C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88113947 | |||||||
| chr4:88114046 | T | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.944-493A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114046 | |||||||
| chr4:88114112 | G | A | 9 | a0002c0004t0001g0012a0002c0004t0001g0206a0002c0004t0001g0207others(6): Show | 9 | HG01071.hp2 HG01169.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.944-559C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114112 | |||||||
| chr4:88114343 | G | A | 4 | a0001c0005t0001g0079a0001c0005t0001g0099a0001c0005t0001g0100others(1): Show | 4 | HG02622.hp1 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.943+614C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114343 | |||||||
| chr4:88114355 | G | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0071others(71): Show | 76 | HG00099.hp1 HG00099.hp2 HG01071.hp2 others(73): Show |
intron_variant | MODIFIER | c.943+602C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114355 | |||||||
| chr4:88114411 | G | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.943+546C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114411 | |||||||
| chr4:88114463 | C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0151a0001c0001t0001g0188 | 3 | HG01243.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.943+494G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114463 | |||||||
| chr4:88114484 | G | A | 2 | a0002c0002t0001g0002a0002c0002t0012g0273 | 3 | HG01257.hp2 HG01258.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.943+473C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114484 | |||||||
| chr4:88114573 | G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0093 | 2 | HG02055.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.943+384C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114573 | |||||||
| chr4:88114627 | C | CA | 10 | a0001c0001t0001g0082a0001c0001t0001g0134a0001c0001t0001g0135others(7): Show | 10 | HG01123.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.943+329dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114627 | |||||||
| chr4:88114627 | CA | C | 51 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0072others(48): Show | 51 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.943+329delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114627 | |||||||
| chr4:88114818 | A | G | 6 | a0001c0001t0001g0076a0001c0001t0001g0090a0001c0001t0001g0097others(3): Show | 6 | HG01109.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.943+139T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 8/15 | chr4 | 88114818 | |||||||
| chr4:88115201 | C | T | 128 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0053others(125): Show | 131 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.842-143G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115201 | |||||||
| chr4:88115231 | A | AGTCTCTC others(9): Show |
9 | a0001c0001t0001g0022a0001c0001t0001g0080a0001c0001t0001g0082others(6): Show | 9 | HG00099.hp1 HG01123.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.842-189_842-174dup others(16): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115231 | |||||||
| chr4:88115232 | G | GTCTCTCT others(11): Show |
3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG01167.hp1 HG01169.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.842-175_842-174ins others(18): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(13): Show |
2 | a0001c0001t0001g0131a0001c0001t0001g0151 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.842-175_842-174ins others(20): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(15): Show |
26 | a0001c0001t0001g0075a0001c0001t0001g0088a0001c0001t0001g0089others(23): Show | 26 | HG00735.hp2 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(22): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(17): Show |
4 | a0001c0001t0001g0015a0001c0001t0001g0107a0001c0001t0001g0118others(1): Show | 4 | HG01884.hp1 HG02738.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(24): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(19): Show |
9 | a0001c0001t0001g0031a0001c0001t0001g0076a0001c0001t0001g0090others(6): Show | 9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(26): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(21): Show |
7 | a0001c0001t0001g0106a0001c0001t0001g0278a0001c0001t0001g0322others(4): Show | 7 | HG01099.hp2 HG01109.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(28): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(23): Show |
13 | a0001c0001t0001g0200a0001c0001t0001g0277a0001c0005t0001g0100others(10): Show | 14 | HG01255.hp2 HG02717.hp2 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(30): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(25): Show |
19 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0231others(16): Show | 19 | HG00323.hp1 HG01884.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(32): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(27): Show |
16 | a0001c0001t0001g0197a0001c0001t0001g0256a0001c0001t0001g0269others(13): Show | 16 | HG00423.hp2 HG00597.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(34): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(29): Show |
9 | a0001c0001t0001g0176a0001c0001t0001g0219a0001c0001t0001g0238others(6): Show | 9 | HG00438.hp2 HG01256.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(36): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(31): Show |
8 | a0001c0001t0001g0172a0001c0001t0001g0257a0001c0001t0001g0279others(5): Show | 8 | HG02273.hp2 HG02300.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(38): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(33): Show |
9 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0127others(6): Show | 9 | HG00621.hp1 HG01516.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(40): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(35): Show |
6 | a0001c0001t0001g0194a0001c0001t0001g0234a0001c0001t0001g0268others(3): Show | 6 | HG01261.hp1 HG02148.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-175_842-174ins others(42): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(37): Show |
2 | a0001c0001t0001g0174a0001c0001t0001g0221 | 2 | NA19011.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.842-175_842-174ins others(44): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115232 | G | GTCTCTCT others(39): Show |
1 | a0002c0002t0001g0002 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.842-175_842-174ins others(46): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115232 | |||||||
| chr4:88115234 | C | CTCTCTCT others(7): Show |
42 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(39): Show | 43 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.842-177_842-176ins others(14): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115234 | |||||||
| chr4:88115236 | C | CTCTCTCT others(5): Show |
2 | a0001c0001t0001g0211a0001c0001t0014g0116 | 2 | HG04184.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.842-179_842-178ins others(12): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115236 | |||||||
| chr4:88115238 | C | CTCTCTCT others(3): Show |
3 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0005g0087 | 3 | HG01243.hp1 NA18968.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.842-181_842-180ins others(10): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115238 | |||||||
| chr4:88115248 | C | G | 147 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0026others(144): Show | 150 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.842-190G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115248 | |||||||
| chr4:88115256 | C | A | 26 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0119others(23): Show | 27 | HG00735.hp2 HG01099.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.842-198G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(19): Show |
1 | a0001c0001t0001g0274 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(26): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(15): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0114 | 2 | HG01069.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(22): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(25): Show |
1 | a0001c0001t0008g0341 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(32): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(17): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0102a0001c0001t0001g0147 | 3 | HG00642.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.842-199_842-198ins others(24): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(23): Show |
1 | a0001c0001t0006g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(30): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(25): Show |
2 | a0001c0001t0008g0340a0002c0002t0002g0246 | 2 | HG00621.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(32): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0325 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(28): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(23): Show |
1 | a0001c0001t0001g0027 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(30): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(27): Show |
1 | a0001c0001t0001g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(34): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(35): Show |
1 | a0002c0002t0001g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(42): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(21): Show |
2 | a0001c0001t0001g0275a0001c0001t0001g0324 | 2 | HG03540.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(28): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(23): Show |
4 | a0001c0001t0001g0026a0001c0001t0001g0321a0002c0002t0002g0059others(1): Show | 4 | HG02015.hp1 HG02080.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(30): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(25): Show |
3 | a0001c0005t0001g0099a0002c0002t0002g0035a0002c0004t0001g0323 | 3 | HG01952.hp2 HG03139.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(32): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(31): Show |
2 | a0001c0001t0004g0335a0002c0002t0001g0057 | 2 | HG02723.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(38): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(23): Show |
1 | a0001c0001t0001g0025 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(30): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(25): Show |
9 | a0002c0002t0002g0009a0002c0002t0002g0014a0002c0002t0002g0016others(6): Show | 9 | HG00438.hp1 HG00597.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(32): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(27): Show |
5 | a0001c0001t0001g0192a0002c0002t0002g0199a0002c0004t0001g0207others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(34): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(29): Show |
2 | a0001c0001t0001g0007a0001c0001t0001g0204 | 2 | HG02055.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(36): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(37): Show |
1 | a0003c0003t0003g0006 | 2 | NA18942.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(44): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(25): Show |
7 | a0001c0001t0001g0223a0001c0001t0001g0263a0002c0002t0002g0017others(4): Show | 8 | HG01074.hp2 HG01943.hp1 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(32): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(27): Show |
4 | a0001c0001t0001g0152a0002c0002t0001g0242a0003c0003t0001g0212others(1): Show | 4 | HG00639.hp2 HG01074.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(34): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(29): Show |
6 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0230others(3): Show | 6 | HG01257.hp1 HG02004.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(36): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(31): Show |
2 | a0003c0003t0001g0217a0003c0003t0001g0288 | 2 | HG02027.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(38): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(33): Show |
1 | a0003c0003t0001g0297 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(40): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(37): Show |
1 | a0003c0003t0003g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(44): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(39): Show |
1 | a0002c0002t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(46): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(27): Show |
8 | a0001c0001t0001g0083a0001c0001t0004g0336a0001c0001t0004g0337others(5): Show | 8 | HG00544.hp1 HG02083.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(34): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(29): Show |
10 | a0001c0001t0001g0185a0001c0001t0007g0343a0002c0002t0001g0047others(7): Show | 10 | NA18951.hp1 NA18970.hp2 NA18979.hp1 others(7): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(36): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(31): Show |
3 | a0001c0001t0001g0201a0002c0002t0001g0056a0002c0002t0001g0066 | 3 | HG02148.hp2 NA18965.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(38): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(33): Show |
3 | a0001c0001t0001g0317a0002c0002t0001g0067a0002c0002t0002g0061 | 3 | HG01981.hp2 HG03225.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(40): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(35): Show |
1 | a0002c0002t0001g0266 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(42): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(37): Show |
3 | a0003c0003t0003g0250a0003c0003t0003g0251a0003c0003t0003g0253 | 3 | HG02071.hp1 NA18939.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.842-199_842-198ins others(44): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(39): Show |
1 | a0003c0003t0003g0262 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(46): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(43): Show |
1 | a0003c0003t0003g0252 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(50): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(29): Show |
5 | a0001c0001t0001g0184a0001c0001t0001g0226a0002c0002t0002g0052others(2): Show | 5 | HG01071.hp2 HG01346.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(36): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(31): Show |
9 | a0001c0001t0001g0254a0002c0004t0001g0248a0003c0003t0001g0290others(6): Show | 9 | HG01433.hp1 HG02040.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(38): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(33): Show |
3 | a0001c0001t0001g0259a0002c0002t0001g0064a0002c0002t0001g0070 | 3 | HG02132.hp2 HG03017.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.842-199_842-198ins others(40): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(35): Show |
1 | a0003c0003t0004g0334 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(42): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(37): Show |
1 | a0003c0003t0003g0313 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(44): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(31): Show |
3 | a0001c0001t0001g0258a0002c0002t0001g0063a0004c0006t0001g0240 | 3 | HG01109.hp1 NA18975.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(38): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(33): Show |
3 | a0001c0001t0001g0177a0001c0001t0001g0205a0002c0002t0002g0245 | 3 | HG00741.hp1 HG02273.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.842-199_842-198ins others(40): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(35): Show |
2 | a0001c0001t0001g0093a0001c0001t0001g0193 | 2 | HG03579.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(42): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(39): Show |
1 | a0002c0002t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(46): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(41): Show |
1 | a0001c0001t0001g0053 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(48): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(43): Show |
1 | a0001c0001t0001g0062 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(50): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(33): Show |
2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG01081.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.842-199_842-198ins others(40): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(35): Show |
2 | a0001c0001t0001g0282a0001c0001t0001g0316 | 2 | NA18906.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(42): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(37): Show |
2 | a0001c0001t0001g0111a0002c0002t0001g0065 | 2 | HG01928.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.842-199_842-198ins others(44): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(39): Show |
1 | a0001c0001t0001g0233 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(46): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(49): Show |
1 | a0001c0001t0001g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(56): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(35): Show |
6 | a0001c0001t0001g0126a0001c0001t0001g0161a0001c0001t0001g0175others(3): Show | 6 | HG00423.hp1 HG01978.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.842-199_842-198ins others(42): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(37): Show |
1 | a0001c0001t0001g0077 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(44): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(37): Show |
3 | a0001c0001t0001g0222a0001c0001t0001g0243a0002c0002t0002g0069 | 3 | HG00544.hp2 HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.842-199_842-198ins others(44): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(39): Show |
1 | a0001c0001t0001g0229 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(46): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(45): Show |
1 | a0002c0002t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(52): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(47): Show |
1 | a0002c0002t0004g0332 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.842-199_842-198ins others(54): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | C | CTCTCTCT others(41): Show |
1 | a0001c0001t0013g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.842-199_842-198ins others(48): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115256 | CTA | C | 3 | a0001c0001t0001g0028a0001c0001t0005g0181a0006c0012t0001g0030 | 3 | HG00639.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.842-200_842-199del others(2): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115256 | |||||||
| chr4:88115258 | A | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.842-200T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115258 | |||||||
| chr4:88115260 | A | C | 46 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.842-202T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115260 | |||||||
| chr4:88115262 | A | C | 16 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0024others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.842-204T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115262 | |||||||
| chr4:88115264 | A | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0155others(2): Show | 5 | HG00741.hp2 HG03239.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.842-206T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115264 | |||||||
| chr4:88115266 | A | C | 2 | a0001c0001t0001g0174a0001c0001t0014g0116 | 2 | HG04184.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.842-208T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115266 | |||||||
| chr4:88115268 | A | C | 1 | a0001c0001t0014g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.842-210T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115268 | |||||||
| chr4:88115270 | A | C | 1 | a0001c0001t0014g0116 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.842-212T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115270 | |||||||
| chr4:88115283 | T | A | 1 | a0002c0002t0001g0042 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.842-225A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115283 | |||||||
| chr4:88115284 | A | ATT | 24 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0172others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.842-227_842-226ins others(2): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115284 | |||||||
| chr4:88115284 | A | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0053others(140): Show | 147 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.842-226T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115284 | |||||||
| chr4:88115287 | T | G | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.842-229A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115287 | |||||||
| chr4:88115344 | G | T | 2 | a0002c0002t0001g0055a0002c0002t0001g0057 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.842-286C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115344 | |||||||
| chr4:88115535 | C | T | 1 | a0002c0002t0002g0061 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.842-477G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115535 | |||||||
| chr4:88115621 | C | CA | 40 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0071others(37): Show | 41 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.842-564dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115621 | |||||||
| chr4:88115621 | CAAAAAAA | C | 34 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(31): Show | 34 | HG00609.hp1 HG00621.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.842-570_842-564del others(7): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115621 | |||||||
| chr4:88115700 | G | C | 1 | a0001c0001t0001g0234 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.842-642C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115700 | |||||||
| chr4:88115803 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.842-745A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88115803 | |||||||
| chr4:88116082 | C | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG00323.hp2 HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.842-1024G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88116082 | |||||||
| chr4:88116120 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.842-1062C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88116120 | |||||||
| chr4:88116126 | T | C | 48 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0075others(45): Show | 48 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.842-1068A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88116126 | |||||||
| chr4:88116173 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.842-1115G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88116173 | |||||||
| chr4:88116303 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.842-1245C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88116303 | |||||||
| chr4:88116466 | G | A | 336 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.842-1408C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88116466 | |||||||
| chr4:88116516 | AAAAAAAT others(329): Show |
A | 336 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.841+1257_842-1459d others(2): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88116516 | |||||||
| chr4:88116533 | CTTTTTTT others(17): Show |
C | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.842-1499_842-1476d others(26): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88116533 | |||||||
| chr4:88116988 | G | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0071a0001c0001t0001g0080others(38): Show | 42 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.841+1121C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88116988 | |||||||
| chr4:88117169 | C | G | 1 | a0001c0001t0001g0279 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.841+940G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117169 | |||||||
| chr4:88117243 | G | A | 1 | a0003c0003t0001g0302 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.841+866C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117243 | |||||||
| chr4:88117245 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.841+864C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117245 | |||||||
| chr4:88117324 | GA | G | 47 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0075others(44): Show | 47 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.841+784delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117324 | |||||||
| chr4:88117337 | C | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG01884.hp2 HG02145.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.841+772G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117337 | |||||||
| chr4:88117384 | G | T | 1 | a0002c0002t0001g0242 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.841+725C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117384 | |||||||
| chr4:88117387 | C | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0071a0001c0001t0001g0080others(33): Show | 37 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.841+722G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117387 | |||||||
| chr4:88117498 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.841+611T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117498 | |||||||
| chr4:88117562 | G | A | 2 | a0001c0001t0001g0132a0002c0002t0001g0202 | 2 | HG03471.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.841+547C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117562 | |||||||
| chr4:88117579 | G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0151a0001c0001t0001g0188 | 3 | HG01243.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.841+530C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117579 | |||||||
| chr4:88117737 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.841+372T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117737 | |||||||
| chr4:88117821 | C | CTGAGCTT others(7): Show |
1 | a0001c0001t0001g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.841+274_841+287dup others(14): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117821 | |||||||
| chr4:88117930 | A | G | 59 | a0003c0003t0001g0004a0003c0003t0001g0117a0003c0003t0001g0178others(56): Show | 61 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.841+179T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117930 | |||||||
| chr4:88117948 | G | A | 1 | a0001c0001t0010g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.841+161C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88117948 | |||||||
| chr4:88118091 | T | C | 22 | a0001c0001t0001g0075a0001c0001t0001g0088a0001c0001t0001g0089others(19): Show | 22 | HG00735.hp2 HG01069.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.841+18A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 7/15 | chr4 | 88118091 | |||||||
| chr4:88118348 | T | C | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(33): Show | 37 | HG00423.hp2 HG00597.hp2 HG01952.hp1 others(34): Show |
intron_variant | MODIFIER | c.690-88A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88118348 | |||||||
| chr4:88118432 | T | C | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(33): Show | 37 | HG00423.hp2 HG00597.hp2 HG01952.hp1 others(34): Show |
intron_variant | MODIFIER | c.690-172A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88118432 | |||||||
| chr4:88118464 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.690-204C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88118464 | |||||||
| chr4:88118470 | T | C | 1 | a0003c0003t0001g0218 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.690-210A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88118470 | |||||||
| chr4:88118477 | T | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(75): Show | 80 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.690-217A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88118477 | |||||||
| chr4:88118621 | G | T | 2 | a0003c0003t0001g0182a0003c0003t0001g0289 | 2 | HG01255.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.690-361C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88118621 | |||||||
| chr4:88118875 | G | A | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0108others(2): Show | 5 | HG02809.hp2 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-615C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88118875 | |||||||
| chr4:88118952 | G | C | 1 | a0001c0005t0001g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.690-692C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88118952 | |||||||
| chr4:88119165 | C | A | 1 | a0002c0002t0011g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.690-905G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88119165 | |||||||
| chr4:88119444 | G | C | 1 | a0001c0001t0001g0319 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.690-1184C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88119444 | |||||||
| chr4:88119568 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.690-1308C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88119568 | |||||||
| chr4:88119616 | G | GTTT | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.690-1359_690-1357d others(5): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88119616 | |||||||
| chr4:88119698 | A | G | 95 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0062others(92): Show | 96 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.690-1438T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88119698 | |||||||
| chr4:88119701 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.690-1441A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88119701 | |||||||
| chr4:88119755 | T | TAAAAGCA others(343): Show |
1 | a0003c0003t0001g0290 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.690-1496_690-1495i others(352): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88119755 | |||||||
| chr4:88119863 | C | T | 33 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0054others(30): Show | 34 | HG01071.hp2 HG01109.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.690-1603G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88119863 | |||||||
| chr4:88119880 | C | T | 6 | a0002c0002t0002g0032a0002c0002t0002g0033a0002c0002t0002g0041others(3): Show | 6 | NA18612.hp1 NA18747.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-1620G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88119880 | |||||||
| chr4:88119990 | G | A | 1 | a0003c0003t0001g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.689+1645C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88119990 | |||||||
| chr4:88120144 | A | G | 338 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(335): Show | 344 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.689+1491T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88120144 | |||||||
| chr4:88120247 | T | C | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(33): Show | 37 | HG00423.hp2 HG00597.hp2 HG01952.hp1 others(34): Show |
intron_variant | MODIFIER | c.689+1388A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88120247 | |||||||
| chr4:88120440 | A | T | 1 | a0001c0001t0005g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.689+1195T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88120440 | |||||||
| chr4:88120598 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.689+1037G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88120598 | |||||||
| chr4:88120612 | A | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG01074.hp1 HG01257.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.689+1023T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88120612 | |||||||
| chr4:88120725 | G | A | 3 | a0001c0001t0001g0058a0001c0001t0002g0236a0001c0001t0002g0237 | 3 | HG02165.hp2 NA18952.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.689+910C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88120725 | |||||||
| chr4:88120726 | C | T | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(33): Show | 37 | HG00423.hp2 HG00597.hp2 HG01952.hp1 others(34): Show |
intron_variant | MODIFIER | c.689+909G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88120726 | |||||||
| chr4:88120884 | C | A | 1 | a0001c0001t0005g0181 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.689+751G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88120884 | |||||||
| chr4:88121054 | T | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.689+581A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88121054 | |||||||
| chr4:88121431 | C | T | 1 | a0001c0001t0005g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.689+204G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 6/15 | chr4 | 88121431 | |||||||
| chr4:88121808 | T | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(51): Show | 54 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.532-16A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88121808 | |||||||
| chr4:88121901 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.532-109A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88121901 | |||||||
| chr4:88122139 | C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0244 | 2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.532-347G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122139 | |||||||
| chr4:88122167 | C | T | 2 | a0001c0001t0001g0110a0001c0001t0002g0081 | 2 | NA18966.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.532-375G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122167 | |||||||
| chr4:88122239 | A | G | 1 | a0002c0002t0001g0047 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.532-447T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122239 | |||||||
| chr4:88122310 | G | A | 32 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0054others(29): Show | 33 | HG01071.hp2 HG01169.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.532-518C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122310 | |||||||
| chr4:88122332 | G | T | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.532-540C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122332 | |||||||
| chr4:88122343 | G | GTT | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.532-552_532-551ins others(2): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122343 | |||||||
| chr4:88122461 | C | T | 1 | a0002c0002t0002g0033 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.532-669G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122461 | |||||||
| chr4:88122482 | G | C | 59 | a0003c0003t0001g0004a0003c0003t0001g0117a0003c0003t0001g0178others(56): Show | 61 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.532-690C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122482 | |||||||
| chr4:88122633 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.532-841C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122633 | |||||||
| chr4:88122674 | T | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0071others(38): Show | 42 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.532-882A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122674 | |||||||
| chr4:88122729 | G | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.532-937C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122729 | |||||||
| chr4:88122731 | C | G | 2 | a0001c0001t0002g0236a0001c0001t0002g0237 | 2 | NA18952.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.532-939G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122731 | |||||||
| chr4:88122764 | C | T | 2 | a0003c0003t0004g0333a0003c0003t0004g0334 | 2 | HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.532-972G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122764 | |||||||
| chr4:88122801 | G | A | 2 | a0001c0001t0006g0084a0001c0001t0006g0085 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.532-1009C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122801 | |||||||
| chr4:88122862 | T | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(51): Show | 54 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.532-1070A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122862 | |||||||
| chr4:88122915 | T | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0026others(75): Show | 80 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.532-1123A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88122915 | |||||||
| chr4:88123028 | G | C | 59 | a0003c0003t0001g0004a0003c0003t0001g0117a0003c0003t0001g0178others(56): Show | 61 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.532-1236C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88123028 | |||||||
| chr4:88123160 | A | T | 59 | a0003c0003t0001g0004a0003c0003t0001g0117a0003c0003t0001g0178others(56): Show | 61 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.532-1368T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88123160 | |||||||
| chr4:88123361 | C | CCTCCAAG others(52): Show |
1 | a0003c0003t0001g0299 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.532-1628_532-1570d others(61): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88123361 | |||||||
| chr4:88123632 | A | G | 33 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0054others(30): Show | 34 | HG01071.hp2 HG01109.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.532-1840T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88123632 | |||||||
| chr4:88123683 | C | T | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.532-1891G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88123683 | |||||||
| chr4:88123693 | G | A | 1 | a0003c0003t0001g0004 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.532-1901C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88123693 | |||||||
| chr4:88123706 | T | A | 1 | a0002c0002t0002g0038 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.532-1914A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88123706 | |||||||
| chr4:88123754 | C | A | 2 | a0001c0001t0006g0084a0001c0001t0006g0085 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.532-1962G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88123754 | |||||||
| chr4:88124035 | C | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(50): Show | 53 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.532-2243G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88124035 | |||||||
| chr4:88124178 | C | T | 33 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0054others(30): Show | 34 | HG01071.hp2 HG01109.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.532-2386G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88124178 | |||||||
| chr4:88124179 | A | G | 278 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(275): Show | 282 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.532-2387T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88124179 | |||||||
| chr4:88124274 | G | A | 95 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0062others(92): Show | 96 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.532-2482C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88124274 | |||||||
| chr4:88124333 | T | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.532-2541A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88124333 | |||||||
| chr4:88124607 | G | A | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.532-2815C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88124607 | |||||||
| chr4:88124675 | A | G | 1 | a0002c0002t0002g0187 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.532-2883T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88124675 | |||||||
| chr4:88124755 | C | T | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.532-2963G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88124755 | |||||||
| chr4:88124937 | C | T | 2 | a0001c0001t0001g0031a0002c0002t0001g0056 | 2 | HG03471.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.532-3145G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88124937 | |||||||
| chr4:88125017 | G | T | 1 | a0001c0005t0001g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.532-3225C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125017 | |||||||
| chr4:88125050 | C | T | 59 | a0003c0003t0001g0004a0003c0003t0001g0117a0003c0003t0001g0178others(56): Show | 61 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.532-3258G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125050 | |||||||
| chr4:88125061 | G | A | 2 | a0001c0001t0001g0110a0001c0001t0002g0081 | 2 | NA18966.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.532-3269C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125061 | |||||||
| chr4:88125108 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.532-3316G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125108 | |||||||
| chr4:88125142 | A | G | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.532-3350T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125142 | |||||||
| chr4:88125187 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.532-3395C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125187 | |||||||
| chr4:88125243 | G | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0071others(37): Show | 41 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.532-3451C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125243 | |||||||
| chr4:88125249 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.532-3457C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125249 | |||||||
| chr4:88125269 | G | A | 1 | a0001c0001t0010g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.532-3477C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125269 | |||||||
| chr4:88125325 | A | G | 17 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0090others(14): Show | 17 | HG00642.hp2 HG01109.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.532-3533T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125325 | |||||||
| chr4:88125422 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.532-3630G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125422 | |||||||
| chr4:88125423 | G | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0071others(38): Show | 42 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.532-3631C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125423 | |||||||
| chr4:88125465 | G | A | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(33): Show | 37 | HG00423.hp2 HG00597.hp2 HG01952.hp1 others(34): Show |
intron_variant | MODIFIER | c.532-3673C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125465 | |||||||
| chr4:88125477 | G | A | 1 | a0001c0001t0005g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.532-3685C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125477 | |||||||
| chr4:88125607 | C | CA | 10 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0028others(7): Show | 10 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.532-3816dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125607 | C | CAAAAA | 14 | a0001c0001t0001g0053a0001c0001t0001g0077a0001c0001t0001g0092others(11): Show | 14 | HG00099.hp1 HG01123.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.532-3820_532-3816d others(7): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125607 | C | CAAAAAA | 19 | a0001c0001t0001g0003a0001c0001t0001g0071a0001c0001t0001g0096others(16): Show | 20 | HG01175.hp1 HG01256.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.532-3821_532-3816d others(8): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125607 | C | CAAAAAAA | 7 | a0001c0001t0001g0080a0001c0001t0001g0165a0001c0001t0001g0170others(4): Show | 7 | HG00099.hp2 HG01261.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.532-3822_532-3816d others(9): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125607 | C | CAAAAAAA others(1): Show |
12 | a0001c0001t0001g0104a0002c0002t0001g0008a0002c0002t0001g0202others(9): Show | 12 | HG01978.hp2 HG01993.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.532-3823_532-3816d others(10): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125607 | C | CAAAAAAA others(2): Show |
13 | a0002c0002t0001g0034a0002c0002t0001g0040a0002c0002t0001g0242others(10): Show | 13 | HG00423.hp2 HG01952.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.532-3824_532-3816d others(11): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125607 | C | CAAAAAAA others(3): Show |
2 | a0002c0002t0002g0043a0002c0002t0011g0045 | 2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.532-3825_532-3816d others(12): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125607 | C | CAAAAAAA others(4): Show |
9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 10 | HG00597.hp2 HG02027.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.532-3826_532-3816d others(13): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125607 | CA | C | 129 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0082others(126): Show | 133 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.532-3816delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125607 | CAA | C | 65 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0076others(62): Show | 65 | HG00642.hp2 HG00735.hp2 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.532-3817_532-3816d others(4): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125607 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0010g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.532-3828_532-3816d others(15): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125607 | |||||||
| chr4:88125624 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.532-3832T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125624 | |||||||
| chr4:88125751 | G | A | 33 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0054others(30): Show | 34 | HG01071.hp2 HG01109.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.532-3959C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125751 | |||||||
| chr4:88125761 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.532-3969G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125761 | |||||||
| chr4:88125783 | T | A | 95 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0062others(92): Show | 96 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.532-3991A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125783 | |||||||
| chr4:88125934 | G | C | 1 | a0002c0004t0007g0342 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.532-4142C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125934 | |||||||
| chr4:88125948 | G | A | 54 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(51): Show | 54 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.532-4156C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88125948 | |||||||
| chr4:88126017 | T | C | 338 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(335): Show | 344 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.532-4225A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88126017 | |||||||
| chr4:88126021 | A | C | 9 | a0002c0004t0001g0012a0002c0004t0001g0206a0002c0004t0001g0207others(6): Show | 9 | HG01071.hp2 HG01169.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.532-4229T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88126021 | |||||||
| chr4:88126561 | T | C | 1 | a0002c0002t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.531+4500A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88126561 | |||||||
| chr4:88126767 | G | C | 1 | a0001c0001t0005g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.531+4294C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88126767 | |||||||
| chr4:88126870 | A | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0071others(37): Show | 41 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.531+4191T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88126870 | |||||||
| chr4:88126929 | C | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0071others(37): Show | 41 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.531+4132G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88126929 | |||||||
| chr4:88126955 | T | C | 338 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(335): Show | 344 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.531+4106A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88126955 | |||||||
| chr4:88127087 | T | C | 1 | a0002c0002t0011g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.531+3974A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127087 | |||||||
| chr4:88127123 | T | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | HG01106.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.531+3938A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127123 | |||||||
| chr4:88127326 | T | C | 2 | a0001c0001t0001g0110a0001c0001t0002g0081 | 2 | NA18966.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.531+3735A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127326 | |||||||
| chr4:88127450 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.531+3611T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127450 | |||||||
| chr4:88127475 | T | C | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531+3586A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127475 | |||||||
| chr4:88127528 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.531+3533G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127528 | |||||||
| chr4:88127668 | G | A | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531+3393C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127668 | |||||||
| chr4:88127807 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.531+3254G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127807 | |||||||
| chr4:88127903 | T | C | 338 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(335): Show | 344 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.531+3158A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127903 | |||||||
| chr4:88127945 | C | CA | 34 | a0001c0001t0001g0015a0001c0001t0001g0198a0001c0001t0001g0244others(31): Show | 35 | HG01071.hp2 HG01109.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.531+3115dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127945 | |||||||
| chr4:88127955 | G | A | 335 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(332): Show | 341 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.531+3106C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127955 | |||||||
| chr4:88127959 | GA | G | 40 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(37): Show | 41 | HG00423.hp2 HG00597.hp2 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.531+3101delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88127959 | |||||||
| chr4:88128091 | C | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(50): Show | 53 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.531+2970G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128091 | |||||||
| chr4:88128094 | A | C | 1 | a0001c0001t0005g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.531+2967T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128094 | |||||||
| chr4:88128304 | A | G | 1 | a0003c0003t0001g0299 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.531+2757T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128304 | |||||||
| chr4:88128307 | C | A | 1 | a0003c0003t0001g0299 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.531+2754G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128307 | |||||||
| chr4:88128309 | TTTACACT others(27): Show |
T | 1 | a0003c0003t0001g0299 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.531+2718_531+2751d others(36): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128309 | |||||||
| chr4:88128315 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.531+2746G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128315 | |||||||
| chr4:88128346 | T | C | 1 | a0003c0003t0001g0299 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.531+2715A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128346 | |||||||
| chr4:88128347 | T | A | 1 | a0003c0003t0001g0299 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.531+2714A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128347 | |||||||
| chr4:88128348 | G | T | 1 | a0003c0003t0001g0299 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.531+2713C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128348 | |||||||
| chr4:88128375 | G | A | 1 | a0003c0003t0001g0299 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.531+2686C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128375 | |||||||
| chr4:88128378 | T | A | 1 | a0003c0003t0001g0299 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.531+2683A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128378 | |||||||
| chr4:88128402 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.531+2659G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128402 | |||||||
| chr4:88128490 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.531+2571G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128490 | |||||||
| chr4:88128529 | C | G | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531+2532G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128529 | |||||||
| chr4:88128834 | A | T | 1 | a0001c0001t0001g0221 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.531+2227T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128834 | |||||||
| chr4:88128874 | C | A | 59 | a0003c0003t0001g0004a0003c0003t0001g0117a0003c0003t0001g0178others(56): Show | 61 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.531+2187G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128874 | |||||||
| chr4:88128956 | T | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.531+2105A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88128956 | |||||||
| chr4:88129378 | T | C | 1 | a0002c0002t0002g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.531+1683A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88129378 | |||||||
| chr4:88129590 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.531+1471T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88129590 | |||||||
| chr4:88129846 | A | G | 95 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0062others(92): Show | 96 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.531+1215T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88129846 | |||||||
| chr4:88129967 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.531+1094G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88129967 | |||||||
| chr4:88130043 | T | A | 1 | a0001c0001t0005g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.531+1018A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88130043 | |||||||
| chr4:88130052 | C | T | 3 | a0002c0002t0001g0002a0002c0002t0002g0086a0002c0002t0012g0273 | 4 | HG01257.hp2 HG01258.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.531+1009G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88130052 | |||||||
| chr4:88130211 | C | T | 1 | a0001c0001t0010g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.531+850G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88130211 | |||||||
| chr4:88130311 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.531+750G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88130311 | |||||||
| chr4:88130421 | C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0164a0001c0001t0001g0165others(2): Show | 6 | HG00099.hp2 HG01256.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.531+640G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88130421 | |||||||
| chr4:88130488 | T | C | 1 | a0001c0001t0005g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.531+573A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88130488 | |||||||
| chr4:88130586 | C | T | 1 | a0002c0002t0001g0034 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.531+475G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 5/15 | chr4 | 88130586 | |||||||
| chr4:88131598 | A | T | 1 | a0002c0002t0001g0070 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.378+205T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 4/15 | chr4 | 88131598 | |||||||
| chr4:88131720 | T | C | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+83A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 4/15 | chr4 | 88131720 | |||||||
| chr4:88131989 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.264-72G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 3/15 | chr4 | 88131989 | |||||||
| chr4:88131999 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.264-82A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 3/15 | chr4 | 88131999 | |||||||
| chr4:88132137 | A | C | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.264-220T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 3/15 | chr4 | 88132137 | |||||||
| chr4:88132343 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.263+233G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 3/15 | chr4 | 88132343 | |||||||
| chr4:88132499 | G | A | 2 | a0001c0001t0001g0275a0001c0001t0001g0278 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.263+77C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 3/15 | chr4 | 88132499 | |||||||
| chr4:88132504 | C | CA | 6 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0107others(3): Show | 6 | HG02738.hp1 HG03490.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+71dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 3/15 | chr4 | 88132504 | |||||||
| chr4:88132506 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.263+70T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 3/15 | chr4 | 88132506 | |||||||
| chr4:88132566 | T | C | 33 | a0002c0002t0001g0002a0002c0002t0001g0042a0002c0002t0001g0054others(30): Show | 34 | HG01071.hp2 HG01109.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.263+10A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 3/15 | chr4 | 88132566 | |||||||
| chr4:88132638 | G | A | 6 | a0001c0001t0001g0076a0001c0001t0001g0090a0001c0001t0001g0097others(3): Show | 6 | HG01109.hp2 HG02809.hp1 HG02895.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.204-3C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88132638 | |||||||
| chr4:88132728 | A | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0174a0001c0001t0001g0175 | 3 | HG00423.hp1 NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.204-93T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88132728 | |||||||
| chr4:88132856 | G | C | 2 | a0001c0001t0001g0118a0001c0001t0001g0188 | 2 | HG01243.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.204-221C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88132856 | |||||||
| chr4:88133107 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.204-472G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133107 | |||||||
| chr4:88133152 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.204-517G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133152 | |||||||
| chr4:88133180 | T | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(50): Show | 53 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.204-545A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133180 | |||||||
| chr4:88133240 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.204-605C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133240 | |||||||
| chr4:88133334 | C | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(50): Show | 53 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.204-699G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133334 | |||||||
| chr4:88133360 | G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-725C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133360 | |||||||
| chr4:88133364 | G | GA | 10 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0090others(7): Show | 10 | HG00642.hp2 HG01109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.204-730dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133364 | |||||||
| chr4:88133515 | A | G | 57 | a0003c0003t0001g0004a0003c0003t0001g0117a0003c0003t0001g0178others(54): Show | 59 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.204-880T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133515 | |||||||
| chr4:88133586 | G | A | 1 | a0001c0001t0010g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.204-951C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133586 | |||||||
| chr4:88133740 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.204-1105C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133740 | |||||||
| chr4:88133864 | G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0095a0001c0001t0001g0107others(2): Show | 5 | HG02738.hp1 HG03490.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.204-1229C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88133864 | |||||||
| chr4:88134010 | AG | A | 6 | a0001c0001t0001g0082a0001c0001t0001g0134a0001c0001t0001g0135others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.204-1376delC | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134010 | |||||||
| chr4:88134011 | G | A | 326 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(323): Show | 332 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.204-1376C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134011 | |||||||
| chr4:88134042 | C | T | 94 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0062others(91): Show | 95 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.204-1407G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134042 | |||||||
| chr4:88134227 | G | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0071others(32): Show | 36 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.204-1592C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134227 | |||||||
| chr4:88134333 | A | G | 332 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(329): Show | 338 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.204-1698T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134333 | |||||||
| chr4:88134510 | T | C | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.204-1875A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134510 | |||||||
| chr4:88134558 | G | C | 333 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(330): Show | 339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.204-1923C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134558 | |||||||
| chr4:88134677 | G | A | 8 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(5): Show | 8 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.204-2042C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134677 | |||||||
| chr4:88134690 | C | T | 1 | a0002c0004t0001g0208 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.204-2055G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134690 | |||||||
| chr4:88134726 | A | T | 1 | a0001c0001t0001g0209 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.204-2091T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134726 | |||||||
| chr4:88134775 | A | G | 1 | a0001c0001t0005g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.204-2140T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134775 | |||||||
| chr4:88134949 | T | C | 2 | a0002c0002t0001g0171a0002c0002t0004g0332 | 2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.204-2314A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134949 | |||||||
| chr4:88134949 | T | G | 1 | a0002c0002t0002g0281 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.204-2314A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134949 | |||||||
| chr4:88134951 | C | T | 2 | a0001c0001t0006g0084a0001c0001t0006g0085 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.204-2316G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134951 | |||||||
| chr4:88134956 | T | C | 53 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(50): Show | 53 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.204-2321A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88134956 | |||||||
| chr4:88135035 | G | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(50): Show | 53 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.204-2400C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135035 | |||||||
| chr4:88135186 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.204-2551G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135186 | |||||||
| chr4:88135231 | C | T | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-2596G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135231 | |||||||
| chr4:88135275 | T | G | 3 | a0001c0001t0001g0058a0001c0001t0002g0236a0001c0001t0002g0237 | 3 | HG02165.hp2 NA18952.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.204-2640A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135275 | |||||||
| chr4:88135413 | A | C | 2 | a0001c0001t0001g0268a0001c0001t0013g0220 | 2 | HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.204-2778T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135413 | |||||||
| chr4:88135558 | C | T | 1 | a0002c0002t0002g0068 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.204-2923G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135558 | |||||||
| chr4:88135559 | G | A | 1 | a0002c0002t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.204-2924C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135559 | |||||||
| chr4:88135563 | G | A | 35 | a0002c0002t0001g0008a0002c0002t0001g0034a0002c0002t0001g0036others(32): Show | 36 | HG00423.hp2 HG00597.hp2 HG01952.hp1 others(33): Show |
intron_variant | MODIFIER | c.204-2928C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135563 | |||||||
| chr4:88135594 | T | G | 1 | a0001c0001t0007g0343 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.204-2959A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135594 | |||||||
| chr4:88135700 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.204-3065A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135700 | |||||||
| chr4:88135821 | T | G | 4 | a0003c0003t0001g0212a0003c0003t0001g0213a0003c0003t0001g0216others(1): Show | 4 | HG00639.hp2 HG01081.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-3186A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88135821 | |||||||
| chr4:88136109 | T | C | 8 | a0001c0001t0001g0179a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 8 | NA18947.hp2 NA18961.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.204-3474A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136109 | |||||||
| chr4:88136137 | G | T | 1 | a0002c0004t0001g0323 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.204-3502C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136137 | |||||||
| chr4:88136155 | G | T | 2 | a0002c0002t0002g0059a0002c0002t0002g0249 | 2 | HG02015.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.204-3520C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136155 | |||||||
| chr4:88136185 | G | A | 1 | a0001c0001t0004g0338 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.204-3550C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136185 | |||||||
| chr4:88136188 | T | G | 1 | a0001c0001t0001g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.204-3553A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136188 | |||||||
| chr4:88136482 | A | G | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+3311T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136482 | |||||||
| chr4:88136512 | C | T | 90 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0062others(87): Show | 91 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.203+3281G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136512 | |||||||
| chr4:88136533 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.203+3260G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136533 | |||||||
| chr4:88136622 | C | T | 1 | a0001c0001t0010g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.203+3171G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136622 | |||||||
| chr4:88136691 | G | A | 42 | a0001c0001t0001g0015a0001c0001t0001g0075a0001c0001t0001g0076others(39): Show | 42 | HG00642.hp2 HG00735.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.203+3102C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136691 | |||||||
| chr4:88136695 | G | C | 1 | a0001c0001t0005g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.203+3098C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136695 | |||||||
| chr4:88136718 | T | A | 4 | a0001c0001t0001g0238a0004c0006t0001g0239a0004c0006t0001g0240others(1): Show | 4 | HG00438.hp2 NA18962.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+3075A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136718 | |||||||
| chr4:88136788 | G | T | 1 | a0003c0003t0001g0293 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.203+3005C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88136788 | |||||||
| chr4:88137012 | C | CAATAA | 23 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0077others(20): Show | 23 | HG01175.hp2 HG01361.hp1 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.203+2776_203+2780d others(7): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137012 | C | CAATAAAA others(3): Show |
29 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(26): Show | 30 | HG00099.hp1 HG00099.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.203+2771_203+2780d others(12): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137012 | C | CAATAAAA others(8): Show |
18 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0071others(15): Show | 19 | HG00738.hp2 HG01081.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.203+2766_203+2780d others(17): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137012 | C | CAATAAAA others(13): Show |
18 | a0001c0001t0001g0024a0002c0002t0001g0055a0002c0002t0001g0060others(15): Show | 18 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.203+2761_203+2780d others(22): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137012 | C | CAATAAAA others(18): Show |
23 | a0002c0002t0001g0054a0002c0002t0001g0067a0002c0002t0001g0074others(20): Show | 25 | HG00597.hp1 HG00609.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.203+2756_203+2780d others(27): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137012 | C | CAATAAAA others(23): Show |
14 | a0002c0002t0001g0065a0002c0002t0002g0069a0003c0003t0001g0182others(11): Show | 14 | HG00544.hp1 HG01255.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.203+2751_203+2780d others(32): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137012 | C | CAATAAAA others(28): Show |
9 | a0003c0003t0001g0196a0003c0003t0001g0286a0003c0003t0001g0287others(6): Show | 9 | HG01074.hp2 HG01928.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.203+2746_203+2780d others(37): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137012 | C | CAATAAAA others(33): Show |
5 | a0003c0003t0001g0305a0003c0003t0001g0306a0003c0003t0001g0307others(2): Show | 5 | NA18612.hp2 NA18953.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+2741_203+2780d others(42): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137012 | CAATAA | C | 34 | a0001c0001t0001g0110a0001c0001t0001g0158a0001c0001t0001g0189others(31): Show | 35 | HG00423.hp2 HG00738.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.203+2776_203+2780d others(7): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137012 | CAATAAAA others(3): Show |
C | 34 | a0001c0001t0001g0075a0001c0001t0001g0088a0001c0001t0001g0089others(31): Show | 34 | HG00639.hp1 HG00735.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.203+2771_203+2780d others(12): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137012 | CAATAAAA others(8): Show |
C | 28 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0031others(25): Show | 28 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.203+2766_203+2780d others(17): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137012 | |||||||
| chr4:88137060 | T | TAAAATAA others(19): Show |
1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.203+2732_203+2733i others(28): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137060 | |||||||
| chr4:88137068 | A | C | 88 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0062others(85): Show | 89 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.203+2725T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137068 | |||||||
| chr4:88137175 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.203+2618G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137175 | |||||||
| chr4:88137330 | G | T | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.203+2463C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137330 | |||||||
| chr4:88137428 | A | G | 1 | a0003c0003t0001g0291 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.203+2365T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137428 | |||||||
| chr4:88137601 | G | A | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+2192C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137601 | |||||||
| chr4:88137705 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.203+2088T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137705 | |||||||
| chr4:88137892 | T | A | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+1901A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137892 | |||||||
| chr4:88137902 | C | A | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+1891G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137902 | |||||||
| chr4:88137902 | C | T | 4 | a0002c0002t0001g0042a0002c0002t0001g0056a0002c0002t0001g0063others(1): Show | 4 | HG01109.hp1 HG02148.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+1891G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137902 | |||||||
| chr4:88137935 | A | G | 17 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.203+1858T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88137935 | |||||||
| chr4:88138134 | G | A | 332 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(329): Show | 338 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.203+1659C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88138134 | |||||||
| chr4:88138182 | G | A | 333 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(330): Show | 339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.203+1611C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88138182 | |||||||
| chr4:88138667 | C | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0053a0001c0001t0001g0071others(37): Show | 41 | HG00099.hp1 HG00099.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.203+1126G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88138667 | |||||||
| chr4:88138765 | G | A | 125 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(122): Show | 127 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.203+1028C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88138765 | |||||||
| chr4:88138842 | C | G | 1 | a0001c0001t0005g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.203+951G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88138842 | |||||||
| chr4:88138946 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.203+847C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88138946 | |||||||
| chr4:88138959 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.203+834C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88138959 | |||||||
| chr4:88139128 | G | A | 1 | a0002c0002t0002g0061 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.203+665C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88139128 | |||||||
| chr4:88139140 | CA | C | 37 | a0001c0001t0001g0083a0001c0001t0001g0318a0002c0002t0001g0008others(34): Show | 38 | HG00423.hp2 HG00597.hp2 HG01952.hp1 others(35): Show |
intron_variant | MODIFIER | c.203+652delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88139140 | |||||||
| chr4:88139201 | T | G | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.203+592A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88139201 | |||||||
| chr4:88139257 | C | A | 1 | a0001c0001t0001g0241 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.203+536G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88139257 | |||||||
| chr4:88139410 | C | A | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.203+383G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88139410 | |||||||
| chr4:88139539 | C | G | 3 | a0002c0002t0001g0042a0002c0002t0001g0063a0002c0002t0001g0066 | 3 | HG01109.hp1 HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.203+254G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88139539 | |||||||
| chr4:88139599 | C | T | 332 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(329): Show | 338 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.203+194G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88139599 | |||||||
| chr4:88139625 | G | A | 332 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(329): Show | 338 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.203+168C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88139625 | |||||||
| chr4:88139757 | T | C | 68 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0034others(65): Show | 70 | HG00423.hp2 HG00597.hp2 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.203+36A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 2/15 | chr4 | 88139757 | |||||||
| chr4:88140033 | T | C | 1 | a0001c0001t0005g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19-19A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140033 | |||||||
| chr4:88140113 | C | T | 83 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0062others(80): Show | 84 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-19-99G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140113 | |||||||
| chr4:88140142 | T | A | 2 | a0002c0002t0002g0041a0002c0002t0002g0052 | 2 | NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-19-128A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140142 | |||||||
| chr4:88140142 | T | C | 1 | a0010c0010t0001g0260 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-19-128A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140142 | |||||||
| chr4:88140144 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-19-130C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140144 | |||||||
| chr4:88140241 | TAATAAGT others(19): Show |
T | 4 | a0002c0002t0002g0032a0002c0002t0002g0033a0002c0002t0002g0046others(1): Show | 4 | NA18612.hp1 NA18747.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-253_-19-228del others(26): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140241 | |||||||
| chr4:88140256 | T | C | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-242A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140256 | |||||||
| chr4:88140281 | T | A | 2 | a0002c0002t0001g0171a0002c0002t0004g0332 | 2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-19-267A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140281 | |||||||
| chr4:88140397 | T | G | 1 | a0001c0001t0008g0341 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-19-383A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140397 | |||||||
| chr4:88140605 | G | C | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-591C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140605 | |||||||
| chr4:88140608 | C | T | 4 | a0001c0005t0001g0079a0001c0005t0001g0099a0001c0005t0001g0100others(1): Show | 4 | HG02622.hp1 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-594G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140608 | |||||||
| chr4:88140650 | A | G | 29 | a0002c0002t0001g0008a0002c0002t0001g0034a0002c0002t0001g0036others(26): Show | 30 | HG00423.hp2 HG01952.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-636T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140650 | |||||||
| chr4:88140664 | C | T | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-19-650G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140664 | |||||||
| chr4:88140758 | C | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0048a0001c0001t0001g0053others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-19-744G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140758 | |||||||
| chr4:88140923 | A | G | 72 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(69): Show | 72 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.-19-909T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140923 | |||||||
| chr4:88140991 | C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027 | 3 | HG02109.hp1 HG02486.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-19-977G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88140991 | |||||||
| chr4:88141037 | C | T | 63 | a0002c0002t0001g0002a0002c0002t0001g0008a0002c0002t0001g0034others(60): Show | 65 | HG00423.hp2 HG01071.hp2 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.-19-1023G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88141037 | |||||||
| chr4:88141133 | T | G | 139 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(136): Show | 141 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(138): Show |
intron_variant | MODIFIER | c.-19-1119A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88141133 | |||||||
| chr4:88141218 | T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0169 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-19-1204A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88141218 | |||||||
| chr4:88141265 | C | T | 1 | a0002c0002t0011g0045 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-19-1251G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88141265 | |||||||
| chr4:88141361 | G | T | 72 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(69): Show | 72 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.-19-1347C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88141361 | |||||||
| chr4:88141758 | A | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0277a0001c0001t0001g0321 | 3 | HG02717.hp2 HG02922.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-19-1744T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88141758 | |||||||
| chr4:88141798 | G | A | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-1784C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88141798 | |||||||
| chr4:88141890 | A | G | 1 | a0003c0003t0001g0290 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-19-1876T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88141890 | |||||||
| chr4:88141954 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-19-1940T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88141954 | |||||||
| chr4:88142089 | GA | G | 72 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0019others(69): Show | 72 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.-19-2076delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142089 | |||||||
| chr4:88142097 | C | A | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-2083G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142097 | |||||||
| chr4:88142202 | G | A | 29 | a0002c0002t0001g0008a0002c0002t0001g0034a0002c0002t0001g0036others(26): Show | 30 | HG00423.hp2 HG01952.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19-2188C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142202 | |||||||
| chr4:88142211 | G | A | 55 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0072others(52): Show | 55 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.-19-2197C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142211 | |||||||
| chr4:88142321 | G | A | 1 | a0002c0002t0004g0332 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-19-2307C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142321 | |||||||
| chr4:88142322 | A | C | 1 | a0002c0002t0004g0332 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-19-2308T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142322 | |||||||
| chr4:88142504 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-19-2490C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142504 | |||||||
| chr4:88142699 | C | A | 151 | a0001c0001t0001g0048a0001c0001t0001g0058a0001c0001t0001g0062others(148): Show | 154 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-19-2685G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142699 | |||||||
| chr4:88142734 | C | T | 1 | a0001c0001t0004g0335 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-19-2720G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142734 | |||||||
| chr4:88142833 | G | A | 250 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0015others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.-19-2819C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142833 | |||||||
| chr4:88142847 | C | A | 1 | a0001c0001t0010g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19-2833G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142847 | |||||||
| chr4:88142897 | G | A | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-2883C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142897 | |||||||
| chr4:88142942 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-19-2928G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88142942 | |||||||
| chr4:88143208 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-19-3194C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88143208 | |||||||
| chr4:88143224 | G | A | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19-3210C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88143224 | |||||||
| chr4:88143319 | C | G | 4 | a0002c0002t0002g0014a0002c0002t0002g0016a0002c0002t0002g0017others(1): Show | 4 | HG01952.hp1 HG01978.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-3305G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88143319 | |||||||
| chr4:88143429 | A | C | 180 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0082others(177): Show | 183 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-19-3415T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88143429 | |||||||
| chr4:88143450 | C | T | 240 | a0001c0001t0001g0003a0001c0001t0001g0048a0001c0001t0001g0058others(237): Show | 245 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-19-3436G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88143450 | |||||||
| chr4:88143807 | AC | A | 72 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0076others(69): Show | 73 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-19-3794delG | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88143807 | |||||||
| chr4:88143808 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19-3794G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88143808 | |||||||
| chr4:88143865 | T | G | 3 | a0001c0001t0001g0263a0001c0001t0001g0322a0002c0002t0001g0171 | 3 | HG01099.hp2 HG02451.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-19-3851A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88143865 | |||||||
| chr4:88143924 | C | T | 13 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(10): Show | 13 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19-3910G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88143924 | |||||||
| chr4:88144135 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-19-4121C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144135 | |||||||
| chr4:88144155 | C | T | 1 | a0002c0002t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19-4141G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144155 | |||||||
| chr4:88144201 | C | A | 180 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0082others(177): Show | 183 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-19-4187G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144201 | |||||||
| chr4:88144287 | T | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-4273A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144287 | |||||||
| chr4:88144383 | G | A | 2 | a0002c0002t0001g0042a0002c0004t0001g0012 | 2 | HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-19-4369C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144383 | |||||||
| chr4:88144449 | C | CT | 157 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0137others(154): Show | 160 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.-19-4436dupA | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144449 | |||||||
| chr4:88144449 | C | CTT | 18 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(15): Show | 18 | HG00741.hp1 HG01169.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19-4437_-19-4436d others(4): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144449 | |||||||
| chr4:88144449 | CT | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-19-4436delA | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144449 | |||||||
| chr4:88144449 | CTT | C | 8 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0125others(5): Show | 8 | HG02293.hp1 HG03490.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-4437_-19-4436d others(4): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144449 | |||||||
| chr4:88144645 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19-4631C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144645 | |||||||
| chr4:88144705 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-19-4691G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144705 | |||||||
| chr4:88144716 | A | C | 180 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0082others(177): Show | 183 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-19-4702T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144716 | |||||||
| chr4:88144923 | C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0062others(100): Show | 105 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.-19-4909G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144923 | |||||||
| chr4:88144967 | GA | G | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-4954delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88144967 | |||||||
| chr4:88145032 | A | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0108a0001c0001t0006g0150 | 3 | HG02572.hp1 HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-19-5018T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145032 | |||||||
| chr4:88145067 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19-5053C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145067 | |||||||
| chr4:88145115 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-19-5101C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145115 | |||||||
| chr4:88145334 | C | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0108a0001c0001t0006g0150 | 3 | HG02572.hp1 HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-19-5320G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145334 | |||||||
| chr4:88145537 | C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0108a0001c0001t0006g0150 | 3 | HG02572.hp1 HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-19-5523G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145537 | |||||||
| chr4:88145538 | G | A | 1 | a0002c0002t0001g0171 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19-5524C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145538 | |||||||
| chr4:88145563 | C | A | 180 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0082others(177): Show | 183 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-19-5549G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145563 | |||||||
| chr4:88145635 | T | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087 | 3 | HG01243.hp1 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-19-5621A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145635 | |||||||
| chr4:88145795 | C | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087others(1): Show | 4 | HG01243.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-5781G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145795 | |||||||
| chr4:88145806 | G | C | 1 | a0001c0001t0005g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-19-5792C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145806 | |||||||
| chr4:88145837 | C | CGCTGA | 180 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0082others(177): Show | 183 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-19-5824_-19-5823i others(7): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88145837 | |||||||
| chr4:88146080 | T | C | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-6066A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146080 | |||||||
| chr4:88146266 | TG | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0062others(107): Show | 112 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(109): Show |
intron_variant | MODIFIER | c.-19-6253delC | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146266 | |||||||
| chr4:88146340 | G | GT | 180 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0082others(177): Show | 183 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-19-6327_-19-6326i others(3): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146340 | |||||||
| chr4:88146346 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19-6332T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146346 | |||||||
| chr4:88146374 | C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0062others(108): Show | 113 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.-19-6360G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146374 | |||||||
| chr4:88146390 | A | C | 1 | a0001c0001t0016g0331 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-19-6376T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146390 | |||||||
| chr4:88146532 | C | A | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19-6518G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146532 | |||||||
| chr4:88146623 | A | G | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-6609T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146623 | |||||||
| chr4:88146684 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-19-6670C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146684 | |||||||
| chr4:88146729 | C | T | 5 | a0001c0001t0001g0082a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-6715G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146729 | |||||||
| chr4:88146798 | G | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087 | 3 | HG01243.hp1 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-19-6784C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146798 | |||||||
| chr4:88146855 | C | A | 285 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0048others(282): Show | 290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.-19-6841G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146855 | |||||||
| chr4:88146860 | C | T | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-6846G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146860 | |||||||
| chr4:88146898 | AGAAG | A | 285 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0048others(282): Show | 290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.-19-6888_-19-6885d others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146898 | |||||||
| chr4:88146947 | A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG00099.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-19-6933T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146947 | |||||||
| chr4:88146947 | AAGGG | A | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-6937_-19-6934d others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88146947 | |||||||
| chr4:88147016 | G | GGAAA | 31 | a0001c0001t0001g0044a0001c0001t0001g0153a0001c0001t0001g0154others(28): Show | 32 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.-19-7006_-19-7003d others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | G | GGAAAGAA others(1): Show |
7 | a0001c0001t0001g0093a0001c0001t0001g0261a0001c0001t0001g0269others(4): Show | 7 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-7010_-19-7003d others(10): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | G | GGAAAGAA others(5): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG02647.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-19-7014_-19-7003d others(14): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | G | GGAAAGAA others(9): Show |
16 | a0001c0001t0001g0075a0001c0001t0001g0090a0001c0001t0001g0092others(13): Show | 16 | HG00738.hp1 HG01884.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.-19-7018_-19-7003d others(18): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | G | GGAAAGAA others(13): Show |
18 | a0001c0001t0001g0076a0001c0001t0001g0102a0001c0001t0001g0103others(15): Show | 18 | HG00735.hp2 HG01109.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19-7022_-19-7003d others(22): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | G | GGAAAGAA others(17): Show |
21 | a0001c0001t0001g0058a0001c0001t0001g0072a0001c0001t0001g0080others(18): Show | 22 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19-7026_-19-7003d others(26): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | G | GGAAAGAA others(21): Show |
19 | a0001c0001t0001g0077a0001c0001t0001g0115a0001c0001t0001g0118others(16): Show | 19 | HG01175.hp1 HG02080.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.-19-7030_-19-7003d others(30): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | G | GGAAAGAA others(25): Show |
23 | a0001c0001t0001g0062a0001c0001t0001g0082a0001c0001t0001g0122others(20): Show | 23 | HG00099.hp2 HG00642.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-19-7034_-19-7003d others(34): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | G | GGAAAGAA others(29): Show |
14 | a0001c0001t0001g0071a0001c0001t0001g0126a0001c0001t0001g0127others(11): Show | 14 | HG01106.hp1 HG01261.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19-7003_-19-7002i others(38): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | G | GGAAAGAA others(33): Show |
6 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG02027.hp1 HG03831.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-7003_-19-7002i others(42): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | G | GGAAAGAA others(37): Show |
2 | a0001c0001t0001g0003a0002c0002t0001g0070 | 3 | HG01256.hp1 HG01433.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.-19-7003_-19-7002i others(46): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147016 | GGAAA | G | 56 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0173others(53): Show | 56 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.-19-7006_-19-7003d others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147016 | |||||||
| chr4:88147046 | A | AAAGAAAG others(20): Show |
1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19-7033_-19-7032i others(29): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147046 | |||||||
| chr4:88147105 | G | A | 163 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0172others(160): Show | 166 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-19-7091C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147105 | |||||||
| chr4:88147207 | G | A | 1 | a0003c0003t0003g0262 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-19-7193C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147207 | |||||||
| chr4:88147303 | G | T | 173 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0082others(170): Show | 176 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.-19-7289C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147303 | |||||||
| chr4:88147346 | G | A | 163 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0172others(160): Show | 166 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-19-7332C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147346 | |||||||
| chr4:88147369 | C | T | 1 | a0002c0002t0002g0013 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-19-7355G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147369 | |||||||
| chr4:88147585 | T | C | 286 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0048others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.-19-7571A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147585 | |||||||
| chr4:88147586 | G | A | 163 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0172others(160): Show | 166 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-19-7572C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147586 | |||||||
| chr4:88147609 | T | C | 182 | a0001c0001t0001g0007a0001c0001t0001g0048a0001c0001t0001g0082others(179): Show | 185 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.-19-7595A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88147609 | |||||||
| chr4:88148171 | A | T | 1 | a0002c0002t0004g0332 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-19-8157T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148171 | |||||||
| chr4:88148176 | T | C | 5 | a0001c0001t0001g0080a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 5 | HG00099.hp1 HG00642.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19-8162A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148176 | |||||||
| chr4:88148254 | T | C | 162 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0173others(159): Show | 165 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.-19-8240A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148254 | |||||||
| chr4:88148354 | A | T | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19-8340T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148354 | |||||||
| chr4:88148358 | G | A | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-8344C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148358 | |||||||
| chr4:88148375 | T | A | 181 | a0001c0001t0001g0007a0001c0001t0001g0082a0001c0001t0001g0134others(178): Show | 184 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-19-8361A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148375 | |||||||
| chr4:88148378 | T | A | 1 | a0001c0001t0001g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19-8364A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148378 | |||||||
| chr4:88148390 | A | G | 5 | a0001c0001t0001g0082a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-8376T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148390 | |||||||
| chr4:88148479 | T | G | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19-8465A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148479 | |||||||
| chr4:88148520 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-19-8506G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148520 | |||||||
| chr4:88148532 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-19-8518C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148532 | |||||||
| chr4:88148572 | C | T | 1 | a0002c0002t0001g0008 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19-8558G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88148572 | |||||||
| chr4:88149101 | G | A | 5 | a0001c0001t0001g0082a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-9087C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149101 | |||||||
| chr4:88149238 | A | C | 1 | a0001c0001t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-20+9148T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149238 | |||||||
| chr4:88149240 | A | G | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+9146T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149240 | |||||||
| chr4:88149305 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-20+9081G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149305 | |||||||
| chr4:88149503 | T | C | 1 | a0008c0008t0001g0049 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-20+8883A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149503 | |||||||
| chr4:88149532 | G | A | 95 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0071others(92): Show | 96 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.-20+8854C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149532 | |||||||
| chr4:88149533 | C | G | 95 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0071others(92): Show | 96 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.-20+8853G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149533 | |||||||
| chr4:88149574 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-20+8812C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149574 | |||||||
| chr4:88149612 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-20+8774C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149612 | |||||||
| chr4:88149639 | G | A | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+8747C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149639 | |||||||
| chr4:88149695 | T | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087others(1): Show | 4 | HG01243.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+8691A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149695 | |||||||
| chr4:88149710 | G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087others(1): Show | 4 | HG01243.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+8676C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149710 | |||||||
| chr4:88149792 | G | A | 1 | a0002c0002t0004g0332 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-20+8594C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149792 | |||||||
| chr4:88149873 | G | A | 1 | a0002c0002t0004g0332 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-20+8513C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149873 | |||||||
| chr4:88149950 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+8436G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149950 | |||||||
| chr4:88149951 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+8435G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149951 | |||||||
| chr4:88149952 | G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087others(1): Show | 4 | HG01243.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+8434C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149952 | |||||||
| chr4:88149952 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+8434C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149952 | |||||||
| chr4:88149953 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+8433C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149953 | |||||||
| chr4:88149954 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+8432G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149954 | |||||||
| chr4:88149955 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+8431G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149955 | |||||||
| chr4:88149956 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+8430G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149956 | |||||||
| chr4:88149958 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+8428G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149958 | |||||||
| chr4:88149992 | G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0173 | 3 | HG02055.hp2 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-20+8394C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88149992 | |||||||
| chr4:88150017 | C | T | 6 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087others(3): Show | 6 | HG01243.hp1 HG01981.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+8369G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150017 | |||||||
| chr4:88150057 | G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087others(1): Show | 4 | HG01243.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+8329C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150057 | |||||||
| chr4:88150186 | G | A | 7 | a0001c0001t0001g0075a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG00735.hp2 HG01884.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+8200C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150186 | |||||||
| chr4:88150202 | T | C | 2 | a0003c0003t0004g0333a0003c0003t0004g0334 | 2 | HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+8184A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150202 | |||||||
| chr4:88150412 | A | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087others(1): Show | 4 | HG01243.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+7974T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150412 | |||||||
| chr4:88150528 | G | C | 2 | a0003c0003t0004g0333a0003c0003t0004g0334 | 2 | HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+7858C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150528 | |||||||
| chr4:88150583 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-20+7803G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150583 | |||||||
| chr4:88150819 | A | G | 2 | a0003c0003t0001g0195a0003c0003t0001g0196 | 2 | HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-20+7567T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150819 | |||||||
| chr4:88150866 | C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087others(1): Show | 4 | HG01243.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+7520G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150866 | |||||||
| chr4:88150907 | C | T | 1 | a0002c0004t0001g0012 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-20+7479G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150907 | |||||||
| chr4:88150970 | C | T | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+7416G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88150970 | |||||||
| chr4:88151221 | A | G | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+7165T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88151221 | |||||||
| chr4:88151468 | G | A | 29 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0071others(26): Show | 30 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.-20+6918C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88151468 | |||||||
| chr4:88151510 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+6876T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88151510 | |||||||
| chr4:88151511 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+6875C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88151511 | |||||||
| chr4:88151594 | T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-20+6792A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88151594 | |||||||
| chr4:88151614 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-20+6772G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88151614 | |||||||
| chr4:88151656 | G | A | 103 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0071others(100): Show | 104 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.-20+6730C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88151656 | |||||||
| chr4:88151761 | T | C | 2 | a0003c0003t0004g0333a0003c0003t0004g0334 | 2 | HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+6625A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88151761 | |||||||
| chr4:88152024 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+6362A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152024 | |||||||
| chr4:88152025 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+6361G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152025 | |||||||
| chr4:88152026 | A | C | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-20+6360T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152026 | |||||||
| chr4:88152045 | A | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0155a0001c0001t0001g0156others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20+6341T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152045 | |||||||
| chr4:88152083 | G | A | 1 | a0001c0001t0016g0331 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-20+6303C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152083 | |||||||
| chr4:88152137 | T | C | 6 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0005g0087others(3): Show | 6 | HG00597.hp2 HG01243.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+6249A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152137 | |||||||
| chr4:88152518 | G | A | 1 | a0001c0001t0016g0331 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-20+5868C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152518 | |||||||
| chr4:88152547 | G | C | 6 | a0001c0001t0001g0080a0001c0001t0001g0143a0001c0001t0001g0144others(3): Show | 6 | HG00099.hp1 HG00642.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+5839C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152547 | |||||||
| chr4:88152556 | T | C | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+5830A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152556 | |||||||
| chr4:88152696 | A | G | 7 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 7 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+5690T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152696 | |||||||
| chr4:88152697 | T | C | 7 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 7 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20+5689A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152697 | |||||||
| chr4:88152712 | G | T | 1 | a0002c0002t0002g0011 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-20+5674C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152712 | |||||||
| chr4:88152718 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-20+5668C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152718 | |||||||
| chr4:88152761 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-20+5625T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152761 | |||||||
| chr4:88152773 | G | T | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+5613C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152773 | |||||||
| chr4:88152775 | A | G | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+5611T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152775 | |||||||
| chr4:88152805 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-20+5581C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152805 | |||||||
| chr4:88152820 | G | T | 73 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(70): Show | 73 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.-20+5566C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152820 | |||||||
| chr4:88152827 | T | C | 238 | a0001c0001t0001g0007a0001c0001t0001g0072a0001c0001t0001g0075others(235): Show | 241 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(238): Show |
intron_variant | MODIFIER | c.-20+5559A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152827 | |||||||
| chr4:88152852 | T | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0058others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-20+5534A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152852 | |||||||
| chr4:88152864 | C | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0081 | 2 | NA18966.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-20+5522G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152864 | |||||||
| chr4:88152879 | A | G | 5 | a0001c0001t0001g0193a0001c0001t0004g0335a0001c0001t0004g0336others(2): Show | 5 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+5507T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152879 | |||||||
| chr4:88152892 | T | A | 1 | a0003c0003t0001g0315 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-20+5494A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152892 | |||||||
| chr4:88152903 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+5483T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152903 | |||||||
| chr4:88152906 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+5480T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152906 | |||||||
| chr4:88152907 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+5479A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152907 | |||||||
| chr4:88152908 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20+5478A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152908 | |||||||
| chr4:88152995 | T | G | 5 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(2): Show | 5 | HG01123.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20+5391A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88152995 | |||||||
| chr4:88153187 | G | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0148a0001c0001t0001g0155others(9): Show | 12 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20+5199C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153187 | |||||||
| chr4:88153253 | T | C | 160 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0019others(157): Show | 163 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.-20+5133A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153253 | |||||||
| chr4:88153282 | A | G | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(2): Show | 5 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+5104T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153282 | |||||||
| chr4:88153292 | T | C | 2 | a0003c0003t0004g0333a0003c0003t0004g0334 | 2 | HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+5094A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153292 | |||||||
| chr4:88153365 | A | G | 1 | a0002c0002t0004g0332 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-20+5021T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153365 | |||||||
| chr4:88153394 | T | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0058others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-20+4992A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153394 | |||||||
| chr4:88153395 | T | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0058others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-20+4991A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153395 | |||||||
| chr4:88153398 | T | G | 1 | a0002c0002t0002g0051 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-20+4988A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153398 | |||||||
| chr4:88153451 | A | G | 164 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(161): Show | 167 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.-20+4935T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153451 | |||||||
| chr4:88153508 | G | T | 189 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0155others(186): Show | 193 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.-20+4878C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153508 | |||||||
| chr4:88153515 | G | A | 164 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(161): Show | 167 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.-20+4871C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153515 | |||||||
| chr4:88153522 | C | T | 163 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(160): Show | 166 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-20+4864G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153522 | |||||||
| chr4:88153527 | C | T | 163 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(160): Show | 166 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-20+4859G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153527 | |||||||
| chr4:88153534 | T | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0058others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-20+4852A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153534 | |||||||
| chr4:88153535 | T | G | 170 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0173others(167): Show | 173 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.-20+4851A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153535 | |||||||
| chr4:88153541 | T | C | 169 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0173others(166): Show | 172 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.-20+4845A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153541 | |||||||
| chr4:88153542 | G | C | 169 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0173others(166): Show | 172 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.-20+4844C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153542 | |||||||
| chr4:88153557 | T | G | 191 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0155others(188): Show | 195 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.-20+4829A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153557 | |||||||
| chr4:88153619 | C | G | 163 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(160): Show | 166 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-20+4767G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153619 | |||||||
| chr4:88153636 | A | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0155a0001c0001t0001g0156others(16): Show | 20 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.-20+4750T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153636 | |||||||
| chr4:88153656 | A | G | 296 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0058others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-20+4730T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153656 | |||||||
| chr4:88153664 | A | C | 2 | a0003c0003t0004g0333a0003c0003t0004g0334 | 2 | HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+4722T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153664 | |||||||
| chr4:88153684 | T | A | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+4702A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153684 | |||||||
| chr4:88153761 | A | G | 1 | a0002c0002t0004g0332 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-20+4625T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153761 | |||||||
| chr4:88153877 | G | A | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+4509C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153877 | |||||||
| chr4:88153879 | A | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0164a0001c0001t0001g0165others(6): Show | 10 | HG00099.hp2 HG01256.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20+4507T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153879 | |||||||
| chr4:88153884 | T | C | 6 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(3): Show | 6 | HG00639.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20+4502A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88153884 | |||||||
| chr4:88154014 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-20+4372A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154014 | |||||||
| chr4:88154051 | T | C | 2 | a0002c0002t0002g0280a0002c0002t0002g0281 | 2 | HG02083.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-20+4335A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154051 | |||||||
| chr4:88154071 | T | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0058others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-20+4315A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154071 | |||||||
| chr4:88154087 | T | C | 35 | a0001c0001t0001g0282a0003c0003t0001g0182a0003c0003t0001g0283others(32): Show | 35 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.-20+4299A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154087 | |||||||
| chr4:88154089 | G | C | 1 | a0003c0003t0003g0313 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-20+4297C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154089 | |||||||
| chr4:88154200 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-20+4186G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154200 | |||||||
| chr4:88154416 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20+3970T>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154416 | |||||||
| chr4:88154471 | C | A | 163 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(160): Show | 166 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.-20+3915G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154471 | |||||||
| chr4:88154614 | G | C | 2 | a0003c0003t0004g0333a0003c0003t0004g0334 | 2 | HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+3772C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154614 | |||||||
| chr4:88154627 | G | A | 1 | a0004c0006t0001g0314 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-20+3759C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154627 | |||||||
| chr4:88154690 | A | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0009c0009t0001g0186 | 3 | NA18970.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-20+3696T>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154690 | |||||||
| chr4:88154702 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-20+3684C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154702 | |||||||
| chr4:88154770 | G | A | 1 | a0001c0005t0001g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-20+3616C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154770 | |||||||
| chr4:88154850 | G | A | 3 | a0001c0001t0004g0339a0001c0001t0016g0331a0002c0002t0004g0332 | 3 | HG03041.hp2 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-20+3536C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154850 | |||||||
| chr4:88154874 | T | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0164a0001c0001t0001g0165others(6): Show | 10 | HG00099.hp2 HG01256.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20+3512A>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154874 | |||||||
| chr4:88154890 | G | C | 1 | a0003c0003t0001g0315 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-20+3496C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154890 | |||||||
| chr4:88154917 | G | A | 2 | a0003c0003t0004g0333a0003c0003t0004g0334 | 2 | HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+3469C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154917 | |||||||
| chr4:88154981 | C | T | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+3405G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88154981 | |||||||
| chr4:88155048 | G | C | 1 | a0001c0001t0001g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-20+3338C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88155048 | |||||||
| chr4:88155304 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-20+3082C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88155304 | |||||||
| chr4:88155626 | C | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-20+2760G>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88155626 | |||||||
| chr4:88155626 | C | T | 2 | a0001c0001t0007g0343a0002c0004t0007g0342 | 2 | NA19000.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-20+2760G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88155626 | |||||||
| chr4:88155733 | C | T | 2 | a0001c0001t0010g0078a0001c0005t0001g0079 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-20+2653G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88155733 | |||||||
| chr4:88155887 | G | A | 1 | a0001c0001t0004g0339 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-20+2499C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88155887 | |||||||
| chr4:88155977 | T | C | 2 | a0003c0003t0004g0333a0003c0003t0004g0334 | 2 | HG01981.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-20+2409A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88155977 | |||||||
| chr4:88156141 | G | A | 4 | a0001c0001t0004g0335a0001c0001t0004g0336a0001c0001t0004g0337others(1): Show | 4 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+2245C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156141 | |||||||
| chr4:88156268 | G | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | NA18961.hp1 NA18988.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-20+2118C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156268 | |||||||
| chr4:88156273 | G | T | 1 | a0003c0003t0003g0183 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-20+2113C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156273 | |||||||
| chr4:88156329 | C | G | 162 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(159): Show | 165 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.-20+2057G>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156329 | |||||||
| chr4:88156370 | C | CA | 8 | a0001c0001t0001g0053a0001c0001t0001g0151a0001c0001t0001g0152others(5): Show | 8 | HG01074.hp1 HG01257.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+2015dupT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156370 | |||||||
| chr4:88156370 | C | CAA | 6 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0005g0181others(3): Show | 6 | HG00639.hp1 HG01943.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20+2014_-20+2015d others(4): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156370 | |||||||
| chr4:88156370 | C | CAAA | 158 | a0001c0001t0001g0003a0001c0001t0001g0164a0001c0001t0001g0165others(155): Show | 162 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-20+2013_-20+2015d others(5): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156370 | |||||||
| chr4:88156370 | C | CAAAA | 8 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0324others(5): Show | 8 | HG00621.hp1 HG01099.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+2012_-20+2015d others(6): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156370 | |||||||
| chr4:88156370 | CA | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0076a0001c0001t0001g0077others(5): Show | 8 | HG02055.hp2 HG02080.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.-20+2015delT | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156370 | |||||||
| chr4:88156392 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-20+1994T>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156392 | |||||||
| chr4:88156605 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-20+1781C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156605 | |||||||
| chr4:88156726 | T | C | 1 | a0002c0002t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-20+1660A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156726 | |||||||
| chr4:88156821 | C | T | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+1565G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156821 | |||||||
| chr4:88156847 | G | C | 9 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+1539C>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156847 | |||||||
| chr4:88156865 | G | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG00423.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-20+1521C>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156865 | |||||||
| chr4:88156908 | C | T | 25 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0071others(22): Show | 26 | HG01109.hp1 HG01257.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-20+1478G>A | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156908 | |||||||
| chr4:88156988 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-20+1398C>T | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88156988 | |||||||
| chr4:88157201 | ATGACACT others(6): Show |
A | 162 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(159): Show | 165 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.-20+1172_-20+1184d others(15): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88157201 | |||||||
| chr4:88157465 | T | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0164a0001c0001t0001g0165others(6): Show | 10 | HG00099.hp2 HG01256.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20+921A>C | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88157465 | |||||||
| chr4:88157663 | TTCTCATC others(4): Show |
T | 1 | a0001c0001t0016g0331 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-20+712_-20+722del others(11): Show |
ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88157663 | |||||||
| chr4:88157772 | T | C | 296 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0062others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-20+614A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88157772 | |||||||
| chr4:88158234 | T | C | 164 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(161): Show | 167 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.-20+152A>G | ABCG2 | ENSG00000118777.12 | transcript | ENST00000237612.8 | protein_coding | 1/15 | chr4 | 88158234 |